BIP Biomedizinische Instrumente und Produkte GmbH
DE-MF-000010311 · Germany · Türkenfeld
BIP Biomedizinische Instrumente und Produkte GmbH is registered in the European database on medical devices as a manufacturer, with 185 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 185 |
|---|
Among these devices, 184 are declared sterile, 1 reusable.
Devices declared under this manufacturer
- BARD® MAGNUM® Biopsy Needle
- BIP Coaxial Cannula
- BIP Coaxial Cannula MR
- BIP EvoCore® Biopsy Device, reusable
- BIP EvoCore® Biopsy Needle
- BIP EvoCore® T Biopsy Needle
- BIP HistoCore® Biopsy Device, disposable
- BIP HistoCore® T Biopsy Device, disposable
- BIP HistoCore® TX Biopsy Device, disposable with Coaxial Cannula
- UROMED HistoCore® Biopsy Device, disposable
- UROMED HistoCore® T Biopsy Device, disposable
Showing 12 of 185 declared devices.
Catalogue references include CC12160MR, CC16200, CC20250MR, EC16250, HC14130, HC20200.
European nomenclature codes declared: A0102010101, A0102010101,A0102010102, A018003, A0102010102.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 185 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 185 |
|---|---|
| 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: Neither register. BIP Biomedizinische Instrumente und Produkte GmbH was not found in either the U.S. or the Canadian register.