MAVIG GmbH
DE-MF-000006207 · Germany · München
MAVIG GmbH is registered in the European database on medical devices as a manufacturer, with 356 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 356 |
|---|
Most frequent device types declared: GD, OT, RA, RD, RP.
Devices declared under this manufacturer
- Allround Protective Model RA631-SON
- Closed X-ray Protective Cap RA612-STD
- Front Apron Model RA660-LVO ComfortLevio Edition
- Front Apron Model RA660-SON Comfort Special Order Item
- Front Protective Model RA645-SON Twiece Special Order Item
- Gonad Apron Model RP643-STD
- OT - Radiation Protective Shields, Upper Body (including Portegra)
- Protective Dental Apron RD644-SON with Thyroid Protection
- Radiation Protective Cap RA611-SON with Breathable Airflow Strip
- Radiation Protective Coat RP668-SON for Children - Special Order Item
- Testes Protection RP280 for Adults
- Thyroid Shield Model RA614-STD
Showing 12 of 356 declared devices.
Catalogue references include OT50001, OT54001-DR, OT90003, RA614537MA41, RA631-SON, RA645-SON.
European nomenclature codes declared: T0299, T030403, T030499, V9099.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | MAVIG GMBH (DE) · FDA 9680506 |
| Devices in EUDAMED | 356 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 356 |
|---|---|
| Found in the U.S. device database | 206 |
| Share | 57.9 % |
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. MAVIG GmbH is registered in the United States but was not found in the Canadian register.