JOTEC GmbH
Active in EUDAMEDGermanyfrom SRN EUDAMED SRN DE-MF-000005709
- Devices
- 7
- Registrations
- EUDAMED
At a glance
Market reach
- European Union
- EUDAMED actor
What JOTEC GmbH makes
Jotec GmbH manufactures vascular grafts, specifically the FLOWLINE BIOPORE EPTFE VASCULAR GRAFT, which is a medical device used for vascular procedures.
The FLOWLINE BIOPORE EPTFE VASCULAR GRAFT is classified as a Class II device and is listed in the FDA 510(k) registry. Jotec GmbH is based in the US.
Catalogue
E-vita OPEN NEO Ref 95HG2620L120-C01
Regimes: CE MDD Registry: EUDAMEDE-nside TAAA Multibranch Stent Graft System Ref 65MU382621-4B8866-00
Regimes: CE MDD Registry: EUDAMEDE-nside TAAA Multibranch Stent Graft System Ref 65MU383021-4B8866-00
Regimes: CE MDD Registry: EUDAMEDE-nside TAAA Multibranch Stent Graft System Ref 65MU332621-4B8866-00
Regimes: CE MDD Registry: EUDAMEDE-nside TAAA Multibranch Stent Graft System Ref 65MU333021-4B8866-00
Regimes: CE MDD Registry: EUDAMEDFlowNit Bioseal Textile Vascular Graft Ref 35ST1506
Regimes: CE MDD Registry: EUDAMEDFlowline Biopore Eptfe Vascular Graft Ref K021547
Regimes: 510(k) Registry: 510(k)
Company details
- EUDAMED SRN
- DE-MF-000005709
- EU VAT number
- DE813081198
- EUDAMED status
- Active
- EUDAMED registered name
- JOTEC GmbH
- EUDAMED abbreviated name
- JOTEC
- Registered address
- 23, Lotzenäcker, 72379, Hechingen, Germany
- Website
- www.artivion.com/
- [email protected]
- Phone
- +4974719220
- PRRC contact
- Stefan Menzl
Frequently asked questions
How many devices does JOTEC GmbH have in the registry?
The registry currently lists 7 devices for JOTEC GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list JOTEC GmbH's devices?
Among its 7 most recently registered devices, JOTEC GmbH has devices listed in EUDAMED (6 devices) and FDA 510(k) (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do JOTEC GmbH's devices fall under?
Among its 7 most recently registered devices, the classes recorded for JOTEC GmbH's devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from JOTEC GmbH in the registry?
The most recently registered devices listed for JOTEC GmbH include E-vita OPEN NEO, E-nside TAAA Multibranch Stent Graft System, FlowNit Bioseal Textile Vascular Graft and FLOWLINE BIOPORE EPTFE VASCULAR GRAFT.