Philipp Kirsch GmbH
DE-MF-000005605 · Germany · Willstätt-Sand
Philipp Kirsch GmbH is registered in the European database on medical devices as a manufacturer, with 31 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 31 |
|---|
Among these devices, 31 are declared active.
Devices declared under this manufacturer
- BL 100 PRO-ACTIVE F
- BL 300 PRO-ACTIVE F
- BL 520 PRO-ACTIVE E
- BL 520 ULTIMATE F
- BL 720 PRO-ACTIVE E
- BL 720 PRO-ACTIVE F
- BL 720 ULTIMATE F
- FROSTER BL 178 PRO-ACTIVE F
- FROSTER BL 180 PRO-ACTIVE F
- FROSTER BL 330 PRO-ACTIVE F
- FROSTER BL 330 ULTIMATE E
- FROSTER BL 530 PRO-ACTIVE E
Showing 12 of 31 declared devices.
Catalogue references include 10209, 10230, 10231, 10485, 12160, 12171.
European nomenclature codes declared: Z121701, Z121702.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | PHILIPP KIRSCH GMBH (DE) · FDA 3043616309 |
| Devices in EUDAMED | 31 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 31 |
|---|---|
| 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. Philipp Kirsch GmbH is registered in the United States but was not found in the Canadian register.