Henrotek A/S
Active in EUDAMEDDenmarkfrom SRN EUDAMED FDA SRN DK-MF-000029313 FEI 3028012839
- Devices
- 5
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
HenroCup® Lid Large Lid for straw Ref Ref no. 12882
Regimes: CE MDR Registry: EUDAMEDHenroCup® Institution Ref Ref no. 12885
Regimes: CE MDR Registry: EUDAMEDHenroCup® Institution with ml. Ref Ref no. 12884
Regimes: CE MDR Registry: EUDAMEDHenroCup® Clear with ml. Ref Ref no. 12877
Regimes: CE MDR Registry: EUDAMEDHenroCup® Ref Ref no. 12878
Regimes: CE MDR Registry: EUDAMED
Company details
- EUDAMED SRN
- DK-MF-000029313
- FDA FEI number
- 3028012839
- EU VAT number
- 12483503
- EUDAMED status
- Active
- EUDAMED registered name
- Henrotek A/S
- Registered address
- 5, Vestermarksvej, 6630, Rødding, Denmark
- Website
- www.henrotek.com
- [email protected]
- Phone
- +45 70 70 78 85
- PRRC contact
- Klaus Jørgensen
Frequently asked questions
How many devices does Henrotek A/S have in the registry?
The registry currently lists 5 devices for Henrotek A/S. Devices recorded under merged duplicate company entries are counted once.
Which registries list Henrotek A/S's devices?
Among its 5 most recently registered devices, Henrotek A/S has devices listed in EUDAMED (5 devices).
What risk classes do Henrotek A/S's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Henrotek A/S's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Henrotek A/S in the registry?
The most recently registered devices listed for Henrotek A/S include HenroCup® Lid Large Lid for straw, HenroCup® Institution, HenroCup® Institution with ml. and HenroCup® Clear with ml..