- Role
- Country
- Date of registration
- Address
Page 5 of 5 — Products 101–108 of 108
| Product | Trade name | Reference / catalog number | Quantity | Status | |
|---|---|---|---|---|---|
| Trial INITIALE Revision femoral stem N° 402 - 200 mm | Trial INITIALE Revision femoral stem N° 402 - 200 mm | 2-0120420 | 03701089533058 | 1 | On the market |
| Trial INITIALE Revision femoral stem N° 402 - 250 mm | Trial INITIALE Revision femoral stem N° 402 - 250 mm | 2-0120425 | 03701089533065 | 1 | On the market |
| Trial INITIALE Revision femoral stem N° 402 - 300 mm | Trial INITIALE Revision femoral stem N° 402 - 300 mm | 2-0120430 | 03701089533072 | 1 | On the market |
| Trial INITIALE Revision femoral stem N° 501 - 200 mm | Trial INITIALE Revision femoral stem N° 501 - 200 mm | 2-0120520 |
03701089533089 |
| 1 |
| On the market |
| Trial INITIALE Revision femoral stem N° 501 - 250 mm | Trial INITIALE Revision femoral stem N° 501 - 250 mm | 2-0120525 | 03701089533096 | 1 | On the market |
| Trial INITIALE Revision femoral stem N° 501 - 300 mm | Trial INITIALE Revision femoral stem N° 501 - 300 mm | 2-0120530 | 03701089533102 | 1 | On the market |
| Trial stem extractor | Trial stem extractor | 2-0106700 | 03701089532679 | 1 | On the market |
| 2-0117803 | — | 2-0117803 | 03701089502863 | 1 | On the market |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
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