← Back to catalogue
A. V. Fistula Sets GR-2214E
EUDAMEDClass IIa (EU MDR)
Ref GR-2214EModel A. V. Fistula Sets GR-2214E
Identity
- Device Name
- A. V. Fistula Sets GR-2214E EUDAMED
- Model / Reference
- A. V. Fistula Sets GR-2214E EUDAMEDGR-2214E EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04987488872625 EUDAMED
- Basic UDI-DI
- B-04987488872625 EUDAMED
- EMDN Code
- A010401 ARTERIOVENOUS FISTULA NEEDLES EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Spain EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
A. V. Fistula Sets GR-2214E by Sb-Kawasumi Laboratories, Inc. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-04987488872625 | Class IIa | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Sb-Kawasumi Laboratories, Inc.
- EUDAMED SRN
- JP-MF-000011253
- Authorised Representative
- Medical Technology Promedt Consulting GmbH DE-AR-000000085
Sources (1)
- EUDAMED f7e1e65d-2e81-4869-a14d-c1e7a32cbe7b 61 fields · synced Jul 9, 2026