AS Columbus®
- Primary DI
- 04046963367503
- Brand
- AS Columbus®
- Company
- Aesculap AG
- Model
- NN566Z
- Catalog number
- NN566Z
- Device description
- AS COLUMBUS TIB.HEMI-SP.T2/2+ 4MM RM/LL
- Published
- 2015-09-24
- Public version status
- Update
- Distribution status
- Not in Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | Orthopedic | 2 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 04046963367503 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 04046963367503 | 04046963367503 | 4046963367503 |
GMDN Terms#
| Term | Definition |
|---|---|
| Knee arthroplasty wedge | A sterile device designed to augment the implantation of a knee femur or tibia prosthesis by acting as a space-filler adjacent to the prosthesis, typically to replace lost bone. It is typically made of metal [e.g., cobalt-chrome (Co-Cr), cobalt-chrome-molybdenum (Co-Cr-Mo) or titanium (Ti)]. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 | |
| Device Size Text, specify | 0 | |
| Device Size Text, specify | 0 | |
| Device Size Text, specify | 0 | |
| Device Size Text, specify | 0 |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(888)229-3002 | setworld_orders@aesculap.com |
| +1(800)282-9000 | GUDID.BBMUS_Service@bbraun.com |
Regulatory Flags#
- DUNS number
- 315018218
- Device count
- 1
- Lot or batch
- true
- Expiration date on label
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 04038653177028 | AESCULAP | OG962R | OG962R | 2016-09-23 |
| 04038653177042 | AESCULAP | OG964R | OG964R | 2016-09-23 |
| 04046964694165 | AESCULAP | PL741SU | PL741SU | 2016-09-23 |
| 04046964809392 | AESCULAP | PL739SU | PL739SU | 2016-10-10 |
| 04046964810411 | AESCULAP | PL743SU | PL743SU | 2016-10-10 |
| 04038653434022 | AESCULAP | FT944T | FT944T | 2015-09-24 |
| 04046963417468 | AESCULAP | FT942T | FT942T | 2015-09-24 |
| 04038653042586 | AESCULAP | ET251R | ET251R | 2016-09-23 |
| 04046964227547 | AESCULAP | GF058B | GF058B | 2016-09-23 |
| 04038653148998 | AESCULAP | DO706R | DO706R | 2020-04-21 |
| 04038653105878 | AESCULAP | LS059R | LS059R | 2020-04-21 |
| 04038653106080 | AESCULAP | LS099R | LS099R | 2020-04-21 |
| 04038653034666 | AESCULAP | DE419R | DE419R | 2020-06-17 |
| 04038653034697 | AESCULAP | DE422R | DE422R | 2020-06-17 |
| 04038653105977 | AESCULAP | LS084R | LS084R | 2022-07-29 |
| 04038653199020 | AESCULAP | XG105R | XG105R | 2021-10-15 |
| 04038653199006 | AESCULAP | XG103R | XG103R | 2020-08-24 |
| 04038653199013 | AESCULAP | XG104R | XG104R | 2020-08-24 |
| 04038653460533 | AESCULAP | XG106R | XG106R | 2020-08-24 |
| 04046963000431 | AESCULAP | XG107R | XG107R | 2020-08-24 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 04260056886225 | InterSpace® Knee Mold Tibial Component M | OSARTIS GmbH | JWH | 2026-10-28 |
| 04260056886249 | InterSpace® Knee Mold Tibial Component L | OSARTIS GmbH | JWH | 2026-10-28 |
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| 05056139247804 | Unity Total Knee System | CORIN LTD | JWH | 2026-10-23 |
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| 05056139247828 | Unity Total Knee System | CORIN LTD | JWH | 2026-10-23 |
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