Sterisets International B.V.
NL-MF-000030883 · Netherlands · Oss
Sterisets International B.V. is registered in the European database on medical devices as a manufacturer, with 184 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 184 |
|---|
Devices declared under this manufacturer
- Blanket Adult Tube 217 x 91 cm
- Blanket Pediatric Tube 117 x 56 cm
- Bowl 2000 ml, ø 225 mm, height 90 mm, PP, transparent with graduation
- Drape 2 ply 70 x 90 cm fenestration Ø 10 cm, with split
- Drape 2 ply PE 25 gr/m2 NW 30 gr/m2 60 x 50 cm with adhesive fen 6 x 8
- Drape 2 ply PE 25 gr/m2 NW 30 gr/m2 75 x 90 cm lateral adhesive
- Drape PE/Tissue 70 x 90 cm, blue
- Forceps Catheter tweezer, length 13 cm, plastic (ABS), green
- Jug 1000 ml, 160 x 115 x 126 mm, PP, transparent with handle
- Swab 10 x 10 cm, 30 gr/4 ply NW
- Swab Gauze 7 x 7 cm, 17 thr, flat
- Syringe 3P L Centric 10 ml, grad 0,5 ml bulk Print Water
Showing 12 of 184 declared devices.
Catalogue references include 5021450, 5021740, 5021872, 5062090, 5071030, 5071250.
European nomenclature codes declared: T020199, V0402, A020199, T030301, M0202010102, M020106.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 184 |
| Country of registration | Netherlands |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 184 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
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: Neither register. Sterisets International B.V. was not found in either the U.S. or the Canadian register.