Is this your brand? Sign in to claim ownership.
Sign in to claim this brandAngiomed GmbH & Co. Medizintechnik KG
US
Last updated May 24, 2026
What Angiomed GmbH & Co. Medizintechnik KG makes
Angiomed GmbH & Co. Medizintechnik KG manufactures central/peripheral venous endovascular stent-grafts and bare-metal peripheral venous stents, including the Venovo® and COVERA devices.
The company's products are classified as Class II and Class III medical devices and are listed in the FDA 510(k) and FDA UDI registries. Angiomed GmbH & Co. Medizintechnik KG is based in the US.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What medical devices does Angiomed GmbH & Co. Medizintechnik KG manufacture?
Angiomed GmbH & Co. Medizintechnik KG manufactures central/peripheral venous endovascular stent-grafts and bare-metal peripheral venous stents, including the Venovo® and COVERA devices. These products are designed for vascular interventions.
Where is Angiomed GmbH & Co. Medizintechnik KG based?
Angiomed GmbH & Co. Medizintechnik KG is based in the US. The company operates from this location to develop and distribute its medical devices to healthcare markets.
Which regulatory registries list Angiomed GmbH & Co. Medizintechnik KG's devices?
Angiomed GmbH & Co. Medizintechnik KG's devices are listed in the FDA 510(k) and FDA UDI registries. These listings indicate that the devices meet specific regulatory requirements for marketing in the US.
How are Angiomed GmbH & Co. Medizintechnik KG's devices classified?
Angiomed GmbH & Co. Medizintechnik KG's devices are classified as Class II and Class III medical devices. Class II devices require general controls and special controls, while Class III devices require premarket approval due to higher risk potential.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- crbard.com
- —
- —
- [email protected]
- Phone
- +1(800)321-4254
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 320047483
Catalogue (215)
Page 5 of 5| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Covera | AVFL08040 | FDA UDI | Class III | Active |
| Venovo® | VENUM20060 | FDA UDI | Class III | Active |
| Venovo® | VENUL10060 | FDA UDI | Class III | Active |
| Covera | AVSL10040 | FDA UDI | Class III | Active |
| Venovo® | VENUL14100 | FDA UDI | Class III | Active |
| Covera | AVSM09030 | FDA UDI | Class III | Active |
| Covera | AVFL10060 | FDA UDI | Class III | Active |
| Venovo® | VENUM12140 | FDA UDI | Class III | Active |
| Ostycut® | 17840010 | FDA UDI | Class I | Unknown |
| Covera | AVFM07060 | FDA UDI | Class III | Active |
| Covera | AVFL07040 | FDA UDI | Class III | Active |
| Venovo® | VENUM18100 | FDA UDI | Class III | Active |
| Covera | AVFM09040 | FDA UDI | Class III | Active |
| Covera | AVSM08100 | FDA UDI | Class III | Active |
| Auto-Vac Biopsy Needle | K912892 | FDA 510(k) | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.