MTT GmbH
DE-MF-000005849 · Germany · Lüneburg
MTT GmbH is registered in the European database on medical devices as a manufacturer, with 20 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 20 |
|---|
Most frequent device types declared: Disposable Templates, Reusable HDR Templates, Reusable Needle Guides, Reusable Templates, mechanical articulated arms.
Among these devices, 1 are declared sterile.
Devices declared under this manufacturer
- EndoMotion
- PeriGrid Disposable 18G
- PeriGrid HDR 14G
- PeriGrid HDR 17G
- PeriGrid HDR 17G Special 0.33
- PeriGrid Reusable 13G
- PeriGrid Reusable 14G
- PeriGrid Reusable 16G
- PeriGrid Reusable 17G
- PeriGrid Reusable 18G
- Solid Lock HS
- SolidLock F-500ext
Showing 12 of 20 declared devices.
Catalogue references include HW-001-010, HW-001-011, HW-001-027, HW-005-001, HW-005-004, HW-005-014.
European nomenclature codes declared: A018002, Z129080.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | MTT GMBH (DE) · FDA 3011545155 |
| Devices in EUDAMED | 20 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 20 |
|---|---|
| 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: United States only. MTT GmbH is registered in the United States but was not found in the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
G10 091118 0008 | issued | 2029-08-06 |