Arthrex®
- Primary DI
- 00888867034396
- Brand
- Arthrex®
- Company
- ARTHREX, INC.
- Model
- AR-502-2L
- Catalog number
- AR-502-2L
- Device description
- IBAL PATLOFEM IMPL,SZ 2,LFT
- Published
- 2017-02-15
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Product Codes#
Code, Name table| Code | Name |
|---|
| KRR | PROSTHESIS, KNEE, PATELLO/FEMORAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER |
Product Code Classifications#
Code, Device, Specialty table| Code | Device | Specialty | Class |
|---|
| KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | Orthopedic | 2 |
Identifiers And Packaging#
Identifier, Type, Agency table| Identifier | Type | Agency | Package quantity | Status |
|---|
| 00888867034396 | Primary | GS1 | 0 | |
| M150AR5022L2 | Secondary | HIBCC | 0 | |
Alternate GTIN / UPC / EAN Codes
Source identifier, GTIN-14 normalized, UPC-A table| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|
| 00888867034396 | 00888867034396 | 888867034396 | 0888867034396 |
Regulatory Flags#
- DUNS number
- 131747628
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
Other Devices From This Company#
Other Devices Sharing Product Codes#
Primary DI, Brand, Company table| Primary DI | Brand | Company | Product code | Published |
|---|
| 00888867034662 | Arthrex® | ARTHREX, INC. | KRR | 2017-12-06 |
| 07613327127423 | INSTRUMENT | Howmedica Osteonics Corp. | KRR | 2017-11-24 |
| 07613327127447 | INSTRUMENT | Howmedica Osteonics Corp. | KRR | 2017-11-24 |
| 07613327127461 | INSTRUMENT | Howmedica Osteonics Corp. | KRR | 2017-11-24 |
| 07613327127478 | INSTRUMENT | Howmedica Osteonics Corp. | KRR | 2017-11-24 |
| 07613327127492 | INSTRUMENT | Howmedica Osteonics Corp. | KRR | 2017-11-24 |
| 07613327127508 | INSTRUMENT | Howmedica Osteonics Corp. | KRR | 2017-11-24 |
| 07613327127515 | INSTRUMENT | Howmedica Osteonics Corp. | KRR | 2017-11-24 |
| 07613327127522 | INSTRUMENT | Howmedica Osteonics Corp. | KRR | 2017-11-24 |
| 07613327127539 | INSTRUMENT | Howmedica Osteonics Corp. | KRR | 2017-11-24 |
| 07613327127560 | INSTRUMENT | Howmedica Osteonics Corp. | KRR | 2017-11-24 |
| 07613327049305 | Avon | Howmedica Osteonics Corp. | KRR | 2017-06-19 |
| 00888867106697 | Arthrex® | ARTHREX, INC. | KRR | 2017-02-15 |
| 00888867034372 | Arthrex® | ARTHREX, INC. | KRR | 2017-02-15 |
| 00888867034389 | Arthrex® | ARTHREX, INC. | KRR | 2017-02-15 |
| 00888867034402 | Arthrex® | ARTHREX, INC. | KRR | 2017-02-15 |
| 00888867034570 | Arthrex® | ARTHREX, INC. | KRR | 2017-02-15 |
| 00888867034587 | Arthrex® | ARTHREX, INC. | KRR | 2017-02-15 |
| 00888867034679 | Arthrex® | ARTHREX, INC. | KRR | 2017-02-15 |
| 00888867035546 | Arthrex® | ARTHREX, INC. | KRR | 2017-02-15 |
| 00888867035560 | Arthrex® | ARTHREX, INC. | KRR | 2017-02-15 |
| 00888867035577 | Arthrex® | ARTHREX, INC. | KRR | 2017-02-15 |
| 00888867106840 | Arthrex® | ARTHREX, INC. | KRR | 2017-02-15 |
| 00888867035553 | Arthrex® | ARTHREX, INC. | KRR | 2017-02-15 |
| 07613154557431 | INSTRUMENT | Howmedica Osteonics Corp. | KRR | 2016-09-24 |
| 07613327051094 | INSTRUMENT | Howmedica Osteonics Corp. | KRR | 2016-09-24 |
| 07613327051100 | INSTRUMENT | Howmedica Osteonics Corp. | KRR | 2016-09-24 |
| 07613327051117 | INSTRUMENT | Howmedica Osteonics Corp. | KRR | 2016-09-24 |
| 07613327051124 | INSTRUMENT | Howmedica Osteonics Corp. | KRR | 2016-09-24 |
| 07613327051131 | INSTRUMENT | Howmedica Osteonics Corp. | KRR | 2016-09-24 |
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