Taperloc
Catalogue number 33-103208, listed by Biomet Orthopedics, United States, under Prosthesis, Hip, Hemi-, Acetabular, Cemented, Metal. 1 manufacturer in China is registered for this product code.
1manufacturer
1catalogue number
Who Else Makes It
Registered in Shanghai.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Zimmer (Shanghai) Medical International Trading Co., Ltd. | Shanghai | Shanghai | Exporter | 106 |
Record
| Listed by | Biomet Orthopedics, United States |
|---|---|
| FDA product code | KWB |
| Device type | Prosthesis, Hip, Hemi-, Acetabular, Cemented, Metal |
| Device class | Class 3 |
| Regulation | 21 CFR 888.3370 |
| Premarket notification | Exempt |
| Record published | 2017-07-28 |
| Record revised | 2025-05-30 (version 6) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Sterilisation | Moist Heat or Steam Sterilization |
| Prescription | Prescription only |
| Label carries | lot or batch number |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 33-103208 | 15MM X 115MM | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Taperloc Microplasty HIP System | Biomet Orthopedics | 1 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.