Dufner Instrumente GmbH
DE-MF-000006417 · Germany · Tuttlingen
Dufner Instrumente GmbH is registered in the European database on medical devices as a manufacturer, with 827 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 827 |
|---|
Most frequent device types declared: $30-30012-01, $30-30028-00, $30-30032-00, $30-30043-00, $30-30050-00.
Among these devices, 827 are declared reusable.
Devices declared under this manufacturer
- AUFRICHT Nasal retractor, double end,
- BANDAGE SCISSORS 23.5 CM
- Cawood-Minnesota Retractor 20mm wide, 15 cm long
- DOYEN MALLET 180GR Ø 30 mm, 21 cm
- DOYEN VAGINAL SPECULUM FIG.3 115X45 MM
- Female catheter, 15 cm, 7,33mm
- HEGAR Uterine dilator, Ø 29 mm
- IC LISTER Bandage scissors, angled, 14 cm
- Laryngeal Mirror without handle, fig. 4 18 mm, RHODIUM
- MICTEC HF-cable, connection: Valleylab, 4 m long
- Mallet 1300 gram steel solid 26.5 cm
- Metal Mounting bracket 12 x 20 x 240 mm
Showing 12 of 827 declared devices.
Catalogue references include 26693-22, 26944-32, 28106-02, 28252-03, 28372-30, 44670-14.
European nomenclature codes declared: L03140102, U03010201, V0402, L181003, L149005, L01040102.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | DUFNER INSTRUMENTE GMBH (DE) · FDA 9612278 |
| Devices in EUDAMED | 827 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 827 |
|---|---|
| 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. Dufner Instrumente GmbH is registered in the United States but was not found in the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
G11 019452 0022 | withdrawn | 2026-09-15 |
D1524100003 | issued | 2030-10-16 |