AS ENDURO
- Primary DI
- 04046963177928
- Brand
- AS ENDURO
- Company
- Aesculap AG
- Model
- NB058Z
- Catalog number
- NB058Z
- Device description
- AS ENDURO TIBIA HEMI-WEDGE T2 16MM RL/LM
- Published
- 2015-09-24
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Related Records
Product Codes
| Code | Name |
|---|---|
| KRO | PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| KRO | Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer | Orthopedic | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 04046963177928 | Primary | GS1 | 0 |
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 | |
| 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
- 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
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|---|---|---|---|---|
| 04038653177035 | AESCULAP | OG963R | OG963R | 2016-09-23 |
| 04038653242962 | AESCULAP | DF262R | DF262R | 2020-06-17 |
| 04038653339563 | AESCULAP | JG901 | JG901 | 2025-03-22 |
| 04038653345038 | AESCULAP | JG910 | JG910 | 2020-05-20 |
| 04038653038244 | AESCULAP | DP511R | DP511R | 2020-06-17 |
| 04038653038251 | AESCULAP | DP512R | DP512R | 2020-06-17 |
| 04038653038282 | AESCULAP | DP540R | DP540R | 2020-06-17 |
| 04038653038299 | AESCULAP | DP541R | DP541R | 2020-06-17 |
| 04038653038305 | AESCULAP | DP542R | DP542R | 2020-06-17 |
| 04038653177011 | AESCULAP | OG961R | OG961R | 2016-09-23 |
| 04038653251407 | AESCULAP | OG960R | OG960R | 2016-09-23 |
| 04038653044207 | MIASPAS MINI-ALIF | FF569R | FF569R | 2020-06-17 |
| 04038653044214 | MIASPAS MINI-ALIF | FF571R | FF571R | 2020-06-17 |
| 04038653044252 | MIASPAS MINI-ALIF | FF578R | FF578R | 2020-06-17 |
| 04038653044283 | MIASPAS MINI-ALIF | FF586R | FF586R | 2020-06-17 |
| 04038653117307 | AESCULAP | NH196 | NH196 | 2017-01-27 |
| 04038653117352 | AESCULAP | NH206 | NH206 | 2017-01-27 |
| 04038653118540 | AESCULAP | NK088 | NK088 | 2015-11-11 |
| 04038653118557 | AESCULAP | NK089 | NK089 | 2015-09-24 |
| 04038653118564 | AESCULAP | NK090 | NK090 | 2015-09-24 |
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| 00889024703285 | OSS™ Orthopedic Salvage System | Biomet Orthopedics, LLC | KRO | 2025-12-02 |
| 00889024703322 | OSS™ Orthopedic Salvage System | Biomet Orthopedics, LLC | KRO | 2025-12-02 |
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