Naslund Medical AB
SE-MF-000003509 · Sweden · Huddinge
Naslund Medical AB is registered in the European database on medical devices as a manufacturer, with 48 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIb | 48 |
|---|
Among these devices, 48 are declared sterile, 48 implantable.
Devices declared under this manufacturer
- Gold Anchor
- Gold Anchor MR+
Showing 12 of 48 declared devices.
Catalogue references include 2208-10, 2208-20-B, GA150X-10-B, GA150X-20-B, GA200-20, GA250-10-B.
European nomenclature codes declared: V901699.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | Naslund Medical AB (SE) · FDA 3008191247 |
| Devices in EUDAMED | 48 |
| Country of registration | Sweden |
Device-level evidence
| Devices with a numeric GTIN | 48 |
|---|---|
| Found in the U.S. device database | 48 |
| Share | 100.0 % |
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: United States only. Naslund Medical AB is registered in the United States but was not found in the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
28620158476 | issued | 2027-11-09 |