Managed Health Services (MHS) requires prior authorization as a condition of payment for many services. This Notice contains information regarding such prior authorization requirements and is applicable to all products offered by MHS, with changes effective July 1, 2014.
Refer to the Frequently Asked Questions below for guidance regarding how to obtain prior authorizations from MHS.
1. Quantitative Testing for Drugs of Abuse & Genetic/Molecular Diagnostic Testing
Laboratory providers have experienced a high number of claim denials for both Quantitative Testing for Drugs of
Abuse and Genetic/Molecular Diagnostic Testing due to lack of prior authorization by the ordering provider. MHS will
be requiring laboratory providers to contact ordering providers to verify that a prior authorization number has been obtained for these services. It is the ordering provider’s responsibility to request prior authorization for Quantitative Testing for Drugs of Abuse and Genetic/Molecular Diagnostic Testing services.
2. Specialized Radiation Therapy
MHS will be requiring ordering providers to obtain prior authorization for prior authorization for services categorized as Radiation Oncology. It is the ordering provider’s responsibility to request prior authorization for Intensity Modulation Radiation Therapy, Proton and Neutron Beam Therapy, and Stereotactic Radiotherapy.
3. Durable Medical Equipment
MHS is making updates to our 2014 authorization requirements. Please reference the attached list or visit the provider portal at mhsindiana.com to review HCPC codes that will require authorization for MHS contracted and non-contracted providers.
FREQUENTLY ASKED QUESTIONS How do I determine if a specific service requires prior authorization?
You may determine which specific codes require prior authorization by visiting our Prior Auth PreScreen tool at mhsindiana.com. Just enter the CPT or HCPC code and the PreScreen Tool will advise you whether the service requires prior authorization.
Additionally, enclosed is a spreadsheet which also lists the updated codes in these categories which require prior authorization.
How do I request a prior authorization for these services?
You may submit the prior authorization request by faxing an authorization to 1-866-912-4245. The fax authorization form can be found on our website at mhsindiana.com.
You may call MHS Medical Management at 1-877-647-4848.
You may submit the prior authorization request utilizing our Secure Web Portal at mhsindiana.com. If your request is approved, you will receive verification through the Secure Web Portal. If you are not currently registered on our Secure Web Portal, you may register through a quick and simple process.
What information will I be required to submit in connection with the prior authorization request? CPT or HCPC code
Diagnosis Code
Name, Tax ID number, and NPI number for both the requesting and servicing providers
Medical records to substantiate the need for the service
If you have any questions regarding this information, you may contact Provider Services at 1-877-647-4848 or contact your dedicated Provider Relations Specialist. You may request an electronic copy of the attached code set via the MHS website using the “Contact Us” or “Secure Messaging” functions.
Non-highlighted codes are codes that will require prior authorization as of July 1, 2014. 1. Quantitative Testing for Drugs of Abuse & Genetic/Molecular Diagnostic Testing
Quantitative Testing for Drugs of Abuse
CPT CODE DESCRIPTION
80154 DRUG SCREEN QUANTITATIVE BENZODIAZEPINES
80184 DRUG SCREEN QUANTITATIVE PHENOBARBITAL
82145 AMPHETAMINE OR METHAMPHETAMINE, CHEMICAL, QUANTITATIVE
82205 BARBITURATES; QUANTITATIVE
82520 COCAINE, QUANTITATIVE
82646 DIHYDROCODEINONE
82649 DIHYDROMORPHINONE, QUANTITATIVE
83805 MEPROBAMATE, BLOOD OR URINE
83840 METHADONE
83887 NICOTINE 83925 ASSAY OF OPIATES
83992 PHENCYCLIDINE (PCP)
Genetic/Molecular Diagnostic Testing
CPT CODE DESCRIPTION
81161 DMD DUPLICATION/DELETION ANALYSIS
81200 ASPA GENE
81201 APC GENE ANALYSIS FULL GENE SEQUENCE
81202 APC GENE ANALYSIS KNOWN FAMILIAL VARIANTS
81203 APC GENE ANALYSIS DUPLICATION/DELETION VARIANTS
81205 BCKDHB GENE
81206 BCR/ABL1 GENE MAJOR BP 81207 BCR/ABL1 GENE MINOR BP 81208 BCR/ABL1 GENE OTHER BP
81209 BLM GENE
81210 BRAF GENE
81211 BRCA1&2 SEQ & COM DUP/DEL 81212 BRCA1&2 185&5385&6174 VAR 81213 BRCA1&2 UNCOM DUP/DEL VAR 81214 BRCA1 FULL SEQ & COM DUP/DEL
81215 BRCA1 GENE KNOWN FAM VARIANT
81217 BRCA2 GENE KNOWN FAM VARIANT
81220 CFTR GENE COM VARIANTS
81221 CFTR GENE KNOWN FAM VARIANTS
81222 CFTR GENE DUP/DELET VARIANTS
81223 CFTR GENE FULL SEQUENCE
81224 CFTR GENE INTRON POLY T 81225 CYP2C19 GENE COM VARIANTS
81226 CYP2D6 GENE COM VARIANTS
81227 CYP2C9 GENE COM VARIANTS
81228 CYTOGEN MICRARRAY COPY NMBR
81229 CYTOGEN M ARRAY COPY NO&SNP
81235 EGFR GENE ANALYSIS COMMON VARIANTS
81240 F2 GENE 81241 F5 GENE 81242 FANCC GENE 81243 FMR1 GENE DETECTION 81244 FMR1 GENE CHARACTERIZATION 81245 FLT3 GENE 81250 G6PC GENE 81251 GBA GENE
81252 GJB2 GENE ANALYSIS FULL GENE SEQUENCE 81253 GJB2 GENE ANALYSIS KNOWN FAMILIAL VARIANTS
81254 GJB6 GENE ANALYSIS COMMON VARIANTS
81255 HEXA GENE
81256 HFE GENE
81257 HBA1/HBA2 GENE
81260 IKBKAP GENE
81261 IGH GENE REARRANGE AMP METH
81262 IGH GENE REARRANG DIR PROBE 81263 IGH VARI REGIONAL MUTATION
81264 IGK REARRANGEABN CLONAL POP
81265 STR MARKERS SPECIMEN ANAL
81266 STR MARKERS SPEC ANAL ADDL
81267 CHIMERISM ANAL NO CELL SELEC 81268 CHIMERISM ANAL W/CELL SELECT
81275 KRAS GENE
81280 LONG QT SYND GENE FULL SEQ
81281 LONG QT SYND KNOWN FAM VAR
81282 LONG QT SYN GENE DUP/DLT VAR
81287 MGMT (O-6-methylguanine-DNA methyltransferase) (eg, glioblastoma multiforme), methylation analysis
81290 MCOLN1 GENE
81291 MTHFR GENE
81292 MLH1 GENE FULL SEQ
81293 MLH1 GENE KNOWN VARIANTS
81294 MLH1 GENE DUP/DELETE VARIANT 81295 MSH2 GENE FULL SEQ
81296 MSH2 GENE KNOWN VARIANTS
81297 MSH2 GENE DUP/DELETE VARIANT 81298 MSH6 GENE FULL SEQ
81299 MSH6 GENE KNOWN VARIANTS
81300 MSH6 GENE DUP/DELETE VARIANT
81301 MICROSATELLITE INSTABILITY
81302 MECP2 GENE FULL SEQ
81303 MECP2 GENE KNOWN VARIANT
81304 MECP2 GENE DUP/DELET VARIANT
81310 NPM1 GENE
81315 PML/RARALPHA COM BREAKPOINTS
81316 PML/RARALPHA 1 BREAKPOINT 81317 PMS2 GENE FULL SEQ ANALYSIS 81318 PMS2 KNOWN FAMILIAL VARIANTS 81319 PMS2 GENE DUP/DELET VARIANTS
81321 PTEN GENE ANALYSIS FULL SEQUENCE ANALYSIS 81322 PTEN GENE ANALYSIS KNOWN FAMILIAL VARIANT
81323 PTEN GENE ANALYSIS DUPLICATION/DELETION VARIANT 81324 PMP22 GENE ANAL DUPLICATION/DELETION ANALYSIS 81325 PMP22 GENE ANALYSIS FULL SEQUENCE ANALYSIS 81326 PMP22 GENE ANALYSIS KNOWN FAMILIAL VARIANT
81330 SMPD1 GENE COMMON VARIANTS
81331 SNRPN/UBE3A GENE
81332 SERPINA1 GENE
81341 TRB@ GENE REARRANGE DIRPROBE
81342 TRG GENE REARRANGEMENT ANAL
81350 UGT1A1 GENE
81355 VKORC1 GENE
81370 HLA I & II TYPING LR 81371 HLA I & II TYPE VERIFY LR 81372 HLA I TYPING COMPLETE LR 81373 HLA I TYPING 1 LOCUS LR 81374 HLA I TYPING 1 ANTIGEN LR 81375 HLA II TYPING AG EQUIV LR 81376 HLA II TYPING 1 LOCUS LR 81377 HLA II TYPE 1 AG EQUIV LR 81378 HLA I & II TYPING HR
81379 HLA I TYPING COMPLETE HR 81380 HLA I TYPING 1 LOCUS HR 81381 HLA I TYPING 1 ALLELE HR 81382 HLA II TYPING 1 LOC HR 81383 HLA II TYPING 1 ALLELE HR
81400 MOPATH PROCEDURE LEVEL 1
81401 MOPATH PROCEDURE LEVEL 2
81402 MOPATH PROCEDURE LEVEL 3
81403 MOPATH PROCEDURE LEVEL 4
81404 MOPATH PROCEDURE LEVEL 5
81405 MOPATH PROCEDURE LEVEL 6
81406 MOPATH PROCEDURE LEVEL 7
81407 MOPATH PROCEDURE LEVEL 8
81408 MOPATH PROCEDURE LEVEL 9
81479 UNLISTED MOLELCULAR PATHOLOGY PROCEDURE
81500 ONCO (OVARIAN) BIOCHEMICAL ASSAY TWO PROTEINS 81503 ONCO (OVARIAN) BIOCHEMICAL ASSAY FIVE PROTEINS 81504
ONCOLOGY (TISSUE OF ORIGIN), MICROARRAY GENE EXPRESSION PROFILING OF > 2000 GENES, UTILIZING FORMALIN-FIXED PARAFFIN-EMBEDDED TISSUE, ALGORITHM REPORTED AS TISSUE SIMILARITY SCORES
81506 ENDOCRINOLOGY BIOCHEMICAL ASSAY SEVEN ANAL
81507
FETAL ANEUPLOIDY (TRISOMY 21, 18, AND 13) DNA SEQUENCE ANALYSIS OF SELECTED REGIONS USING MATERNAL PLASMA, ALGORITHM REPORTED AS A RISK SCORE FOR EACH TRISOMY
81509 FETAL CONGENITAL ABNOR ASSAY 3 PROTEINS 81510 FETAL CONGENITAL ABNOR ASSAY THREE ANAL 81511 FETAL CONGENITAL ABNOR ASSAY FOUR ANAL 81512 FETAL CONGENITAL ABNOR ASSAY FIVE ANAL
81599 UNLISTED MULTIANALYTE ASSAY ALGORITHMIC ANALYSIS
83890 MOLECULE ISOLATE
83891 MOLECULE ISOLATE NUCLEIC
83892 MOLECULAR DIAGNOSTICS
83893 MOLECULE DOT/SLOT/BLOT
83894 MOLECULE GEL ELECTROPHOR
83896 MOLECULAR DX; NUCLEIC ACID PROBE EA
83897 MOLECULE NUCLEIC TRANSFER
83898 MOLECULAR DX AMPLIFICATION TARGET EA SEQUENCE 83900 MOLECULAR DX AMP TARGET MULTIPLEX 1ST 2 SEQ 83901 MOLECULAR DX AMP TARGET MULTIPLEX EA ADDL SEQ 83902 MOLECULAR DX; REVERSE TRANSCRIPTION
83903 MOLEC DX; MUTATION SCAN BY PHYS PROP-1 SEGMT EA 83904 MOLEC DX; MUTATION ID-SEQUENCING-1 SGMT EA 83905 MOLEC DX; MUTATION ID-ALLELE SPEC TRANSCRIP-1-EA 83906 MOLEC DX; MUTATION ID-ALLELE SPEC TRANSLAT-1-EA 83907 LYSE CELLS FOR NUCLEIC EXT
83908 MOLECULAR DX AMPLIFICATION SIGNAL EA SEQUENCE 83909 NUCLEIC ACID HIGH RESOLUTE
83912 MOLECULAR DX; INTERPT & REPORT 83913 RNA STABILIZATION
83914 MUTATION ID ENZYMATIC LIG/PRIMER XTN 1 SGM EA 83915 NUCLEOTIDASE 5'-
86812 TISSUE TYPING; HLA TYPING, A, B, OR C (EG, A10, B7, B27), SINGLE ANTIGEN 86813 TISSUE TYPING; HLA TYPING, A, B, AND/OR C (EG, A10, B7, B27), MULTIPLE A 86816 TISSUE TYPING; HLA TYPING, DR/DQ, SINGLE ANTIGEN
86817 TISSUE TYPING; HLA TYPING, DR/DQ, MULTIPLE ANTIGENS 86821 TISSUE TYPING; LYMPHOCYTE CULTURE, MIXED(MLC) 86822 TISSUE TYPING; LYMPHOCYTE CULTURE, PRIMED(PLC) 86825 HLA X-MATCH, NON-CYTOTOXIC
86826 HLA X-MATCH, NON-CYT ADD-ON 86828 HLA CLASS I&II ANTIBODY QUAL
86829 HLA CLASS I/II ANTIBODY QUAL 86830 HLA CLASS I PHENOTYPE QUAL 86831 HLA CLASS II PHENOTYPE QUAL 86832 HLA CLASS I HIGH DEFIN QUAL 86833 HLA CLASS II HIGH DEFIN QUAL 86834 HLA CLASS I SEMIQUANT PANEL 86835 HLA CLASS II SEMIQUANT PANEL
88230 TISS CULTURE NON-NEOPLAS DISORD; LYMPHOCYTE 88233 TISS CULTURE NON-NEOPLAS DISORD; SKIN/SOLID TISS 88235 TISS CULTURE NON-NEOPLAS DISORD; AMNIOTIC FLUID 88237 TISS CULTURE NEOPLAS DISORD; MARROW/BLD CELLS 88239 TISS CULTURE NEOPLAS DISORD; SOLID TUMOR
88240 CRYOPRESERV-FREEZE & STORE CELLS EA CELL LINE 88241 THAWING & EXPANSION FROZEN CELLS EA ALIQUOT 88245 CHROMOSOME ANALY BREAK SYNDROM; SCE 20-25 CELLS
88248 CHROMOSOME ANALY; BASELINE BREAKAGE
88249 CHROMOSOME ANALY BREAK SYNDROM; CLASTOGEN STRESS
88261 CHROMO ANALY; CT 5 CELLS 1 KARYOTYPE W/BANDING 88262 CHROMO ANALY; CT 15-20 CELLS 2 KARYOTYPES W/BAND 88263 CHROMO ANALY; CT 45 CEL MOSAICISM 2 KARYO W/BAND 88264 CHROMOSOME ANALY; ANALY 20-25 CELLS
88267 CHROMO ANALY AMNIO FLUID CT 15 CELLS 1 KARYOTYPE 88269 CHROMO ANALY AMNIO FLUID CELLS CT 6-12 COLONIES 88271 MOLEC CYTOGEN; DNA PROBE EA
88272 MOLEC CYTOGEN; CHROMOSOM IN SITU HYBRID 3-5 CELL 88273 MOLEC CYTOGEN; CHROMOSOM HYBRID 10-30 CELLS 88274 MOLEC CYTOGEN; INTERPHASE IN SITU HYBRID 25-99 88275 MOLEC CYTOGEN; INTERPHASE IN SITU HYBRID 100-300
88280 CHROMOSOME ANALY; ADD KARYOTYPES EA STUDY
88283 CHROMOSOME ANALY; ADD SPECIALIZED BANDING TECH 88285 CHROMOSOME ANALY; ADD CELLS COUNTED EA STUDY 88289 CHROMOSOME ANALY; ADD HIGH RESOLUTION STUDY 88291 CYTOGEN & MOLEC CYTOGEN INTERPT & REPORT 88299 UNLISTED CYTOGENETIC STUDY
88384 RA-BASED EVAL MLT MOLEC PRBS 11 THRU 50 PRBS 88385 RA-BASED EVAL MLT MOLEC PRBS 51 THRU 250 PRBS
88386 RA-BASED EVAL MLT MOLEC PRBS 251 THRU 500 PRBS S3713 KRAS MUTATION ANALYSIS
S3800 GENETIC TESTING FOR AMYOTROPHIC LATERAL SCLEROSIS (ALS) S3818 COMPLETE GENE SEQUENCE ANALYSIS
S3819 COMPLETE GENE SEQUENCE ANALYSIS
S3820 COMPLETED BRCA1 AND BRCA2 GENE SEQUENCE ANALYSIS FOR SUSCEP S3822 SINGLE MUTATION ANALYSIS FOR SUSCE TO BREAST AND OVARION CANCER
S3823 3-MUTATION ANALYSIS FOR SUSCEP/BREAST &OVARION CANCER IN ASHKENAZI INDI S3828 COMPLETE GENE SEQUENCE ANALYSIS, MLH1 GENE
S3829 COMPLETE GENE SEQUENCE ANALYSIS, MLH2 GENE S3830 COMPLETE MLH1 AND MLH2 GENE SEQUENCE ANALYSIS S3831 SINGLE MUTATION ANALYSIS
S3833 COMPLETE APC GENE SEQUENCE ANAL/SUSCEPTIBILITY TO (FAP)
S3834 SINGLE-MUTATION ANALYSIS /SUSCEPTIBILITY TO (FAP)&ATTENUATED FAP S3835 COMPLETE GENE SEQUENCE ANALYSIS FOR CYSTIC FIBROSIS GENETIC TESTING S3837 COMPLETE GENE SEQUENCE ANALYSIS FOR HEMOCHROMATOSIS GENETIC TESTING S3840 DNA ANALYSIS FOR GERMLINE MUTATIONS OF THE RET PROTO-ONCOGENE
S3841 GENETIC TESTING FOR RETINOBLASTOMA
S3842 GENETIC TESTING FOR VON HIPPEL-LINDAU DISEASE
S3843 DNA ANALYSIS OF THE F5 GENE FOR SUSCEP TO FACTOR V LEIDEN THROMBOPHILIA S3844 DNA ANLYSS/CONNEXIN 26 GENE (GJB2)/SUSCEP/CONGENITAL, PRFND DEAFNESS S3845 GENETIC TESTING FOR ALPHA-THALASSEMIA
S3846 GENETCI TESTING FOR HEMOGLOBIN E BETA-THALASSEMIA S3847 GENETIC TESTING FOR TAY-SACHS DISEASE
S3848 GENETIC TESTING FOR GAUCHER DISEASE S3849 GENETIC TESTING FOR NIEMANN-PICK DISEASE S3850 GENETIC TESTING FOR SICKLE CELL ANEMIA S3851 GENETIC TESTING FOR CANAVAN DISEASE
S3852 DNA ANLYS/APOE EPILSON 4 ALLELE FOR SUSCEP ALZHEIMER'S DISEASE S3853 GENETIC TESTING FOR MYOTONIC MUSCULAR DYSTROPHY
Specialized Radiation Therapy CPT
CODE CODE DESCRIPTION
61796 Stereotactic radiosurgery (SRS) (particle beam, gamma ray, or linear accelerator); 1 simple cranial lesion
61797 SRS; each additional cranial lesion, simple 61798 SRS; 1 complex cranial lesion
61799 SRS; each additional cranial lesion, complex 63620 SRS; 1 spinal lesion
63621 SRS; each additional spinal lesion
77301 Intensity modulated radiotherapy (IMRT) plan, including dose-volume histograms for target and critical structure partial tolerance specifications
77338 Multi-leaf collimator (MLC) device(s) for IMRT, design and construction per IMRT plan 77371 Radiation treatment delivery, SRS, complete course of treatment of cranial lesion(s)
consisting of 1 session; multi-source cobalt 60 based
77372 Radiation treatment delivery, SRS, complete course of treatment of cranial lesion(s) consisting of 1 session; linear accelerator based
77373 Stereotactic body radiation therapy (SBRT), treatment delivery, per fraction to 1 or more lesions, including image guidance, entire course not to exceed 5 fractions
77418 Intensity modulated treatment delivery, single or multiple fields/arcs, via narrow spatially and temporally modulated beams, binary, dynamic MLC, per treatment session
77422 High energy neutron radiation treatment delivery; single treatment area using a single port or parallel-opposed ports with no blocks or simple blocking.
77423 High energy neutron radiation treatment delivery; 1 or more isocenter(s) with coplanar or non-coplanar geometry with blocking and/or wedge, and/or compensator(s)
77432 Stereotactic radiation treatment management of cranial lesion(s) (complete course of treatment consisting of one session)
77435 SBRT, treatment management, per treatment course, to one or more lesions, including image guidance, entire course not to exceed 5 fractions
77520 Proton treatment; simple, without compensation 77522 Proton treatment delivery; simple, with compensation 77523 Proton treatment delivery; intermediate
77525 Proton treatment delivery; complex
0073T
Compensator-based beam modulation treatment delivery of inverse planned treatment using 3 or more high resolution (milled or cast) compensator convergent beam modulated fields, per treatment session
G0251
Linear accelerator based SRS, delivery including collimator changes and custom plugging, fractionated treatment, all lesions, per session, maximum five sessions per course of treatment
G0339 Image-guided robotic linear accelerator-based SRS, complete course of therapy in one session or first session of fractionated treatment
G0340
Image-guided robotic linear accelerator-based SRS, delivery including collimator changes and custom plugging, fractionated treatment, all lesions, per session, second through fifth sessions, maximum five sessions per course of treatment
3. Durable Medical Equipment CPT CODE CODE DESCRIPTION
A6501 COMPRS BURN GARMNT BDYSUIT CSTM FAB
A6503 COMPRS BRN GARMNT FCE HOOD CSTM FAB
A6507 COMPRS BRN GARMNT FT KNEE LEN CSTM
A6511 COMPRS BRN GARMNT LW TRNK LEG OPN
A8003 HELMET PROTECTIVE HARD CUSTOM FABR INCL ALL COMPONENTS/ACCESSOR B4224 PARENTERAL NUTRITION ADMIN KIT PER DAY
E0147 WALKER, HEAVY DUTY, MULTIPLE BRAKING SYSTEM, VARIABLE WHEEL RSISTANCE
E0371 NONPWR ADV PRESS REDUC MATRS OVERLAY STAN L/W E0372 PWR AIR MATRS OVERLAY STAN MATRS LENGTH/WIDTH
E0373 NONPWR ADV PRESS REDUC MATRS
E0575 NEBULIZER ULTRASONIC
E0585 NEBULIZER W/COMPRESSOR & HEATER E0604 BREAST PUMP HEAVY DUTY HOSPITAL GRADE E0617 EXT DEFIB W/INTEGRATED ECG ANALY
E0618 APNEA MONITOR W/O RECORDING FEATURE
E0619 APNEA MONITOR W/RECORDING FEATURE
E0781 AMBULATORY INFUSION PUMP 1/MULTI CHAN PT WEARS E0782 INFUS PUMP IMPL NON-PROGMMABLE
E0783 INFUS PUMP SYST IMPLNT PROGRAMABLE (INCL COMPON) E0786 IMPLNT PROGRAM INFUS PUMP REPLCMT
E0791 PARENTERAL INFUSION PUMP STATIONARY 1/MULTICHANL E1050 FULL RECLINE WHEELCHAIR FIX ARM DETACHABLE LEGS E1405 OXYGEN & WATER VAPOR ENRICH W/HEATED DELIVERY E1406 OXYGEN & WATER VAPOR ENRICH WO HEATED DELIVERY E1600 DELIVERY/INSTALL CHARGES RENAL DIALYSIS EQUIP E1610 REVERSE OSMOSIS WATER PURIFICATION SYSTEM E1615 DEIONIZER WATER PURIFICATION SYSTEM
E1801 SPS ELBOW DEVICE
E1802 DYN ADJUSTBL FORARM PRON/SUPIN DEVC E1805 DYN ADJUS WRIST EXTENSION/FLEXION DEVICE E1810 DYN ADJUS KNEE EXTENSION/FLEXION DEVICE E1811 SPS KNEE DEVICE
E1815 DYN ADJUS ANKLE EXTENSION/FLEXION DEVICE E1816 SPS ANKLE DEVICE
E1818 SPS FOREARM DEVICE
E1825 DYN ADJUS FINGER EXTEN/FLEXION DEVICE E1830 DYN ADJUS TOE EXTENSION/FLEXION DEVICE E1840 DYNAMIC ADJUSTABLE SHOULDER FLEXION
E1841 MXIDIR STATIC PROGS STRETCH SHLDR DEVC INCL CUFF
E2000 GASTRIC SUCTION PUMP, HOME MODEL, PORTABLE OR STATIONARY, ELECTRIC E2100 BLOOD GLUCOSE MONITOR WITH INTEGRATED VOICE SYNTHESIZER
E2120 PULSE GNRTR SYS/TYMPANIC TRTMNT OF INNER EAR ENDOLYMPHATIC FLUID
E2227 GEAR REDUCTION DRIVE WHEEL
E2228 MWC ACC WHEELCHAIR BRAKE
E2402 NEG PRESSURE WOUND THERAPY ELECTRICAL PUMP, STATIONARY OR PORTABLE
E2626 SEO MOBILE ARM SUP ATT TO WC E2627 ARM SUPP ATT TO WC RANCHO TY E2628 MOBILE ARM SUPPORTS RECLININ E2629 FRICTION DAMPENING ARM SUPP
E2630 MONOSUSPENSION ARM/HAND SUPP
K0730 CONTROLLED DOSE INHALATION DRUG DELIVERY SYSTEM
L0430 DEWALL POSTURE PROTECTOR
L0632 LSO SAG RIGID FRAME CUST L0700 SPINAL-CERVICAL-THORACIC- L3330 LIFT, ELEVATION, METAL EX L5973 ANK-FOOT SYS DORS-PLANT F
L6709 TERM DEV MECH HAND VOL CLOSE
L7181 ELECTRONIC ELBO SIMULTANEOUS
L8619 REPLACE COCHLEAR PROCESSOR
Q0479 POWER MODULE COMBO VAD, R
Q0480 DRIVER PNEUMATIC VAD, REP Q0481 MICROPRCSR CU ELEC VAD, REP
Q0482 MICROPRCSR CU COMBO VAD, REP
Q0483 MONITOR ELEC VAD, REP
Q0484 MONITOR ELEC OR COMB VAD REP
Q0491 EMR PWR SOURCE COMBO VAD REP
Q0495 CHARGER ELEC/COMBO VAD, REP
Q0496 BATTERY ELEC/COMBO VAD, REP
Q0502 MOBILITY CART PNEUM VAD, REP
Q0503 BATTERY PNEUM VAD REPLACEMNT
Q0504 PWR ADPT PNEUM VAD, REP VEH Q0506 LITH-ION BATT ELEC/PNEUM
Q1003 NTIOL CATEGORY 3
Q4100 SKIN SUBSTITUTE, NOS
Q4114 INTEGRA FLOWABLE WOUND MA
Q4118 MATRISTEM MICROMATRIX