Hermle Labortechnik GmbH
DE-MF-000024779 · Germany · Wehingen
Hermle Labortechnik GmbH is registered in the European database on medical devices as a manufacturer, with 84 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
Most frequent device types declared: FRONTIER, FRONTIER 5000 Series, Non-refrigerated Centrifuges, Refrigerated Centrifuge.
Devices declared under this manufacturer
- Centrifuge Micro 120V FC5513+R02 IVD
- Centrifuge Micro 230V FC5513+R02 IVD
- Centrifuge Micro 230V FC5513L+R06 IVD
- Centrifuge Micro 230V FC5513R IVD
- Centrifuge Multi 100-230V FC5707+R09 IVD
- Centrifuge Multi 230V FC5916 IVD
- Z 207 MK
- Z 207 MK with rotor
- Z 287 A
- Z 32 HK
- Z 327 K
- Z 36 HK
Showing 12 of 84 declared devices.
Catalogue references include 311.00 V07, 313.00 V02, 319.00 V02, 327.00 V01, 333.00 P02, 333.00 V01.
European nomenclature codes declared: W02069003, W02069005.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | HERMLE LABORTECHNIK GMBH (DE) · FDA 3010394461 |
| Devices in EUDAMED | 84 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 84 |
|---|---|
| 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. Hermle Labortechnik GmbH is registered in the United States but was not found in the Canadian register.