AESCULAP
- Primary DI
- 04046963810306
- Brand
- AESCULAP
- Company
- Aesculap AG
- Model
- NX044
- Catalog number
- NX044
- Device description
- PATELLA 3-PEGS P4
- 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
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 |
|---|
| 04046963810306 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|
| 04046963810306 | 04046963810306 | 4046963810306 |
GMDN Terms
| Term | Definition |
|---|
| Cruciate-retaining total knee prosthesis | A sterile implantable artificial substitute for a knee joint typically designed to replace all the articulating surfaces of the damaged/degenerative (e.g., arthritic) joint [total knee arthroplasty (TKA)]; it is designed to be implanted with retention of the posterior cruciate ligament. It typically includes femoral, tibial, and patellar components that articulate and with parts made of metal, ceramic, and/or polyethylene (PE). The device may be implanted with or without bone cement and is typically used in cases where bone stock is good and supporting ligaments provide adequate stability. |
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 | |
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
Other Devices From This Company
Other Devices Sharing Product Codes
| Primary DI | Brand | Company | Product code | Published |
|---|
| 00889024706774 | Biomet® | Biomet Orthopedics, LLC | JWH | 2026-03-12 |
| 00889024706781 | Biomet® | Biomet Orthopedics, LLC | JWH | 2026-03-12 |
| 00889024706798 | Biomet® | Biomet Orthopedics, LLC | JWH | 2026-03-12 |
| 00889024706804 | Biomet® | Biomet Orthopedics, LLC | JWH | 2026-03-12 |
| 00889024706811 | Biomet® | Biomet Orthopedics, LLC | JWH | 2026-03-12 |
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| 00843575127303 | MOBIO™ Total Knee System | B-ONE ORTHO, CORP. | JWH | 2026-03-06 |
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| 00843575127334 | MOBIO™ Total Knee System | B-ONE ORTHO, CORP. | JWH | 2026-03-06 |
| 00843575127341 | MOBIO™ Total Knee System | B-ONE ORTHO, CORP. | JWH | 2026-03-06 |
| 00843575127358 | MOBIO™ Total Knee System | B-ONE ORTHO, CORP. | JWH | 2026-03-06 |
| 00843575127365 | MOBIO™ Total Knee System | B-ONE ORTHO, CORP. | JWH | 2026-03-06 |
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