Skip to content

Terumo Europe N.V.

Active in EUDAMED

Belgiumfrom 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.

AI-generated from registry data, 5 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue359

Newest first, rows 251-300 of 359

Search and filter all 359 devices
Skip device list
  • RADIFOCUS Guide Wire M Non-Vascular Ref NV-PS35183M

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Ultimaster Nagomi Ref DE-RS2712ASM

    Expiring Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Nagomi Ref DE-RS3518ASM

    Expiring Regimes: CE MDR Registry: EUDAMED Class:III
  • RADIFOCUS Guide Wire M Non-Vascular Ref NV-GS35263M

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • RADIFOCUS Guide Wire M Non-Vascular Ref NV-GA35123M

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Ultimaster Nagomi Ref DE-RS2018ASM

    Expiring Regimes: CE MDR Registry: EUDAMED Class:III
  • Outlook - Angiographic catheter Ref RQ-4AL2000M

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • RADIFOCUS Guide Wire M Non-Vascular Ref NV-PA38153M

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Neolus Needle Ref NN-2325RT900

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Ultimaster Nagomi Ref DE-RS2521ASM

    Expiring Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Nagomi Ref DE-RS3021ASM

    Expiring Regimes: CE MDR Registry: EUDAMED Class:III
  • RADIFOCUS Guide Wire M Non-Vascular Ref NV-PA35403M

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Ultimaster Nagomi Ref DE-RS2233ASM

    Expiring Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Nagomi Ref DE-RS2750ASM

    Expiring Regimes: CE MDR Registry: EUDAMED Class:III
  • RADIFOCUS Introducer II Ref RT-R70D10PQ

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Ultimaster Nagomi Ref DE-RS2221ASM

    Expiring Regimes: CE MDR Registry: EUDAMED Class:III
  • K-Pack II Needle Ref KN-3013RBKTI

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Ultimaster Nagomi Ref DE-RS2033ASM

    Expiring Regimes: CE MDR Registry: EUDAMED Class:III
  • K-Pack II Needle Ref KN-2913RBBKTI

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Neolus Needle Ref NN-2316R

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • RADIFOCUS Guide Wire M Non-Vascular Ref NV-PA35153M

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Ultimaster Nagomi Ref DE-RS3515ASM

    Expiring Regimes: CE MDR Registry: EUDAMED Class:III
  • K-Pack Surshield Needle Ref KN-S2713RBZU

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Ultimaster Nagomi Ref DE-RS2524ASM

    Expiring Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Nagomi Ref DE-RS2533ASM

    Expiring Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Tansei Ref DE-RQ3038KSM

    Active Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Tansei Ref DE-RQ4015KSM

    Active Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Tansei Ref DE-RQ3521KSM

    Active Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Tansei Ref DE-RQ3009KSM

    Active Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Tansei Ref DE-RQ2718KSM

    Active Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Tansei Ref DE-RQ2724KSM

    Active Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Tansei Ref DE-RQ3018KSM

    Active Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Tansei Ref DE-RQ2528KSM

    Active Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Tansei Ref DE-RQ2224KSM

    Active Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Tansei Ref DE-RQ2509KSM

    Active Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Tansei Ref DE-RQ2221KSM

    Active Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Tansei Ref DE-RQ2212KSM

    Active Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Tansei Ref DE-RQ2524KSM

    Active Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Tansei Ref DE-RQ2728KSM

    Active Regimes: CE MDR Registry: EUDAMED Class:III
  • 2 x K-Pack II Needle 1 x Terumo Syringe Ref KIT-S02K2125E

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Ultimaster Tansei Ref DE-RQ2218KSM

    Active Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Tansei Ref DE-RQ3012KSM

    Active Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Tansei Ref DE-RQ2238KSM

    Active Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Tansei Ref DE-RQ4033KSM

    Active Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Tansei Ref DE-RQ3028KSM

    Active Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Tansei Ref DE-RQ2533KSM

    Active Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Tansei Ref DE-RQ3528KSM

    Active Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Tansei Ref DE-RQ4018KSM

    Active Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Tansei Ref DE-RQ3512KSM

    Active Regimes: CE MDR Registry: EUDAMED Class:III
  • Ultimaster Tansei Ref DE-RQ3538KSM

    Active Regimes: CE MDR Registry: EUDAMED Class:III

Rows 251-300 of 359

Showing 251-300 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
Phone
+3216381211
PRRC contact
Koen Verhaert(public in EUDAMED)

EUDAMED certificates9

9 certificates9 valid, 0 expiredMDR 9next expiry 30 Nov 2026

EUDAMED certificates (9)

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 Supplemented Expires in 59 days

    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 Expires in 28 days

    Technical documentation EU MDR

    Issued
    24 Nov 2022
    Expires
    30 Nov 2026
  • 3479GB448221124 Expiring Expires in 28 days

    Quality management system EU MDR

    Issued
    24 Nov 2022
    Expires
    30 Nov 2026