Terumo Corp.
Active in EUDAMEDJapanfrom SRN EUDAMED SRN JP-MF-000017478
Site of Terumo Corp.
Terumo Corp. is a medical device manufacturer based in Japan, with 762 devices listed in EUDAMED (EU Class IIa, Class III, Class IIb and IVD Annex II List B) as of 13 Nov 2026.
- Devices
- 762
- Registrations
- EUDAMED
Registry facts
- Registries
- EUDAMED 762
- Device classes
- EU Class IIa 350
- EU Class III 345
- EU Class IIb 38
- EU IVD Annex II List B 18
- EU Class I 11
- Top EMDN categories
- Sites and related companies
- Identifiers
- EUDAMED SRN JP-MF-000017478
- Other registry ID 2828
At a glance
EU certificates
3 of 4 in force. 1 certificate has expired.
Market reach
- European Union
- EUDAMED actor, 4 certificates
What Terumo Corp. makes
Terumo Corp. manufactures the NANOPASS 32.5, a medical device designed for vascular access, specifically intended for peripheral intravenous catheterization in pediatric and adult patients.
The NANOPASS 32.5 is classified as a Class IIa device and is listed in the EU’s eudamed registry. The company is based in Japan.
Catalogue
Search and filter all 762 devicesShowing 1-50 of 762
Company details
- EUDAMED SRN
- JP-MF-000017478
- Other identifier
- 2828
- EUDAMED status
- Active
- EUDAMED registered name
- Terumo Corporation
- Registered address
- 44-1, 2-chome, Hatagaya, 151-0072, Shibuya-ku, Tokyo, Japan
- PRRC contact
- Hiroki Sasagawa
EUDAMED certificates
4 certificates3 valid, 1 expiredMDR 3, IVDR 1next expiry 2 Mar 2027
TÜV Rheinland LGA Products GmbH 0197 4 certificates
- HZ 1485480-1 Active
Quality management system EU MDR
- Issued
- 21 May 2026
- Expires
- 28 May 2030
- Reason
- Add device or group
- IZ 1485480-1 Active
Technical documentation EU MDR
- Issued
- 19 Dec 2022
- Expires
- 18 Dec 2027
- HX 1485480-1 Expiring
Quality management system EU IVDR
- Issued
- 2 Jun 2022
- Expires
- 2 Mar 2027
- HZ 1485480-1 Expired
Quality management system EU MDR
- Issued
- 18 Dec 2024
- Expires
- 28 May 2025
- Reason
- Add device or group
Frequently asked questions
How many devices does TERUMO CORP. have in the registry?
The registry currently lists 762 devices for TERUMO CORP.. Devices recorded under merged duplicate company entries are counted once.
Which registries list TERUMO CORP.'s devices?
Among its 50 most recently registered devices, TERUMO CORP. has devices listed in EUDAMED (50 devices).
What risk classes do TERUMO CORP.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for TERUMO CORP.'s devices are Class IIa and IVD Annex II List B. Each device page shows its own class and authorisation.
What EUDAMED certificates are recorded for TERUMO CORP.?
EUDAMED lists 4 certificates for TERUMO CORP. (quality management system; technical documentation) under MDR and IVDR. 2 are recorded with the status issued. The most recent was issued on 21 May 2026.
What are the newest devices from TERUMO CORP. in the registry?
The most recently registered devices listed for TERUMO CORP. include RADIFOCUS INTRODUCER II, TERUMO SYRINGE WITH NEEDLE, MEDISAFE FIT Smile Blood Glucose Monitoring System Kits and TERUMO SYRINGE.