Arthrex®

Primary DI
00888867232143
Brand
Arthrex®
Company
ARTHREX, INC.
Model
AR-523-B108
Catalog number
AR-523-B108
Device description
PS TIBIAL BEARING, SIZE 1, 8MM, VIT E
Published
2017-02-15
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
MR Conditional
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
HSXPROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER
KRRPROSTHESIS, KNEE, PATELLO/FEMORAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER
MBHPROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HSXProsthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/PolymerOrthopedic2
KRRProsthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/PolymerOrthopedic2
MBHProsthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/PolymerOrthopedic2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00888867232143PrimaryGS10
M150AR523B1081SecondaryHIBCC0

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00888867232143008888672321438888672321430888867232143

GMDN Terms#

Term, Definition table
TermDefinition
Uncoated knee tibia/insert prosthesisA sterile implantable device designed to replace the tibial condyles (tibial component) during primary bicondylar replacement of the knee joint or to replace a dysfunctional knee prosthesis (revision). It is made of metal [e.g., cobalt-chrome (Co-Cr)] and is not coated with a material intended to improve fixation and stability by promoting bone ingrowth; it includes a polyethylene (PE) insert/platform for femoral articulation. Device implantation is intended to be performed with bone cement.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(800)934-4404complaints@arthrex.com

Regulatory Flags#

DUNS number
131747628
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00888867550292Arthrex®AR-6533S-STAR-6533S-ST2026-09-18
00888867550308Arthrex®AR-6533S-XLAR-6533S-XL2026-09-18
00888867550315Arthrex®AR-6534S-STAR-6534S-ST2026-09-18
00888867550322Arthrex®AR-6534S-XLAR-6534S-XL2026-09-18
00888867550339Arthrex®AR-6533S-STSAR-6533S-STS2026-09-18
00888867550346Arthrex®AR-6533S-XLSAR-6533S-XLS2026-09-18
00888867550353Arthrex®AR-6534S-STSAR-6534S-STS2026-09-18
00888867550360Arthrex®AR-6534S-XLSAR-6534S-XLS2026-09-18
00888867550377Arthrex®AR-6534S-14AR-6534S-142026-09-18
00888867550384Arthrex®AR-6534S-17AR-6534S-172026-09-18
00888867552692Arthrex®AR-6533S-XL-14AR-6533S-XL-142026-09-18
00888867552708Arthrex®AR-6533S-ST-14AR-6533S-ST-142026-09-18
00888867552715Arthrex®AR-6534S-ST-14AR-6534S-ST-142026-09-18
00888867552722Arthrex®AR-6533S-XLS-14AR-6533S-XLS-142026-09-18
00888867552739Arthrex®AR-6533S-STS-14AR-6533S-STS-142026-09-18
00888867552746Arthrex®AR-6534S-XL-14AR-6534S-XL-142026-09-18
00888867552753Arthrex®AR-6534S-STS-14AR-6534S-STS-142026-09-18
00888867552760Arthrex®AR-6534S-XLS-14AR-6534S-XLS-142026-09-18
00888867568044Arthrex®AR-9650RAO-05AR-9650RAO-052026-09-17
00888867568051Arthrex®AR-9650RAO-06AR-9650RAO-062026-09-17

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Primary DI, Brand, Company table
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00192629005495ADVANCE®Microport Orthopedics Inc.MBH2026-09-18
00192629005501ADVANCEMicroport Orthopedics Inc.MBH2026-09-18
00192629005518ADVANCEMicroport Orthopedics Inc.MBH2026-09-18
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