Stille AB
SE-MF-000001228 · Sweden · Torshälla
Stille AB is registered in the European database on medical devices as a manufacturer, with 149 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 149 |
|---|
Most frequent device types declared: 102-9020, 102-9020-15, 102-9022, 102-9030-15, 102-9062-17.
Among these devices, 100 are declared reusable, 14 active.
Devices declared under this manufacturer
- ADSON STILLE DRESSING FORCEPS
- ADSON STILLE TISSUE FORCEPS
- CRAFOORD-STILLE DRESSING FORCEPS
- Catheter Tray
- DANDY STILLE ARTERY FORCEPS
- Medstone detachable side rail EU
- Medstone detachable side rail US W
- STILLE DRESSING FORCEPS
- STILLE TISSUE FORCEPS
- STILLE VASCULAR FORCEPS DeBAKEY
- Side rail
- Side rail non symetrical Left EU
Showing 12 of 149 declared devices.
Catalogue references include 102-9020-15, 102-9062-17, 102-9300, 102-9322, 103-10310, 505-1129.
European nomenclature codes declared: L031308, Z12011280, L031306, Z12011202, L031399, V08060199.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | STILLE AB (SE) · FDA 3003696170 |
| Devices in EUDAMED | 149 |
| Country of registration | Sweden |
Device-level evidence
| Devices with a numeric GTIN | 149 |
|---|---|
| Found in the U.S. device database | 134 |
| Share | 89.9 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: United States only. Stille AB is registered in the United States but was not found in the Canadian register.