2 catalogue numbers from 01.04441.010, listed by Zimmer, Inc., United States, under Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer + Additive, Cemented. 2 manufacturers in China are registered for this product code.
Who Else Makes It
Concentrated in Shanghai (1), Jiangsu (1).
Record
Regulatory record for Ashcom™ Shoulder | Listed by | Zimmer, Inc., United States |
| FDA product code | PAO |
| Device type | Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer + Additive, Cemented |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3660 |
| Establishment | Contract manufacturer, Specification developer, Repacker / relabeller, Manufacturer, Exporter |
| Record published | 2017-07-27 |
| Record revised | 2023-06-27 (version 3) |
Specifications
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, manufacturing date |
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.