Terumo Europe N.V.
Active in EUDAMEDBelgiumfrom SRN EUDAMED FDA SRN BE-MF-000001434 FEI 3001570557
- Devices
- 359
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
What Terumo Europe N.V. makes
Terumo Europe N.V. makes medical devices such as the Ultimaster Tansei.
The company's portfolio includes devices classified as Class II, Class IIa, and Class III, and is listed in registries such as eudamed and fda_510k, with the company based in Belgium.
Catalogue
Search and filter all 359 devicesDeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
27 G X 1/2 K-Pack Surshield Needle Ref K111797
Regimes: 510(k) Registry: 510(k)Venoject Luer Adapter Ref K041358
Regimes: 510(k) Registry: 510(k)Terumo Injection Filter Needle (NF-3013RBKE05M) Ref K230951
Regimes: 510(k) Registry: 510(k)Surflo Winged Infusion Set Ref K070362
Regimes: 510(k) Registry: 510(k)SurGuard3 Safety Hypodermic Needle Ref K212095
Regimes: 510(k) Registry: 510(k)2 x K-Pack II Needle 1 x Terumo Syringe Ref KIT-S01K2125E
Regimes: CE MDR Registry: EUDAMED2 x K-Pack II Needle 1 x Terumo Syringe Ref KIT-S01K2123E
Regimes: CE MDR Registry: EUDAMED
Showing 351-359 of 359
Company details
- EUDAMED SRN
- BE-MF-000001434
- SRN (system / procedure pack)
- BE-PR-000001431
- FDA FEI number
- 3001570557
- EU VAT number
- BE 0408 270 327
- EUDAMED status
- Active
- EUDAMED registered name
- TERUMO EUROPE N.V.
- Registered address
- 40, Interleuvenlaan, 3001, Leuven, Belgium
- [email protected]
- Phone
- +3216381211
- PRRC contact
- Koen Verhaert
EUDAMED certificates
9 certificates9 valid, 0 expiredMDR 9next expiry 30 Nov 2026
TÜV Rheinland LGA Products GmbH 0197 6 certificates
- IZ 1594584-5 Active
Technical documentation EU MDR
- Issued
- 16 Oct 2025
- Expires
- 15 Oct 2030
- IZ 1594584-3 Active
Technical documentation EU MDR
- Issued
- 23 Aug 2025
- Expires
- 22 Aug 2030
- IZ 1594584-4 Active
Technical documentation EU MDR
- Issued
- 17 Jun 2025
- Expires
- 16 Jun 2030
- IZ 1594584-2 Active
Technical documentation EU MDR
- Issued
- 9 May 2025
- Expires
- 8 May 2030
- IZ 1594584-1 Active
Technical documentation EU MDR
- Issued
- 14 Apr 2025
- Expires
- 13 Apr 2030
- HZ 1594584-1 Expiring
Quality management system EU MDR
- Issued
- 23 Aug 2025
- Expires
- 31 Dec 2026
- Reason
- Other
DNV MEDCERT GmbH 0482 3 certificates
- 13090GB450250128 Active
Technical documentation EU MDR
- Issued
- 28 Jan 2025
- Expires
- 27 Jan 2030
- 20232GB450221124 Expiring
Technical documentation EU MDR
- Issued
- 24 Nov 2022
- Expires
- 30 Nov 2026
- 3479GB448221124 Expiring
Quality management system EU MDR
- Issued
- 24 Nov 2022
- Expires
- 30 Nov 2026