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ULTRAMED A.V. FISTULA NEEDLE 17 G (Single)
EUDAMEDClass IIa (EU MDR)
Ref 9003-17/SModel ULTRAMED A.V. FISTULA NEEDLE 17 G (Single)Model ULTRAMED A.V. FISTULA NEEDLE
Identity
- Trade Name
- ULTRAMED A.V. FISTULA NEEDLE 17 G (Single) EUDAMED
- Device Name
- ULTRAMED A.V. FISTULA NEEDLE EUDAMED
- Model / Reference
- ULTRAMED A.V. FISTULA NEEDLE 17 G (Single) EUDAMED9003-17/S EUDAMEDULTRAMED A.V. FISTULA NEEDLE EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06223004250385 EUDAMED
- Basic UDI-DI
- B-06223004250385 EUDAMED622300425AVF9003RQ EUDAMED
- EMDN Code
- A010401 ARTERIOVENOUS FISTULA NEEDLES EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Türkiye EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
ULTRAMED A.V. FISTULA NEEDLE 17 G (Single) by Ultra For Medical Products (Ultramed) U.M.I.C (S.A.E) — Class IIa — MDR, MDD — listed in EUDAMED
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | B-06223004250385 | Class IIa | Active |
| EUDAMED | European Union | CE/MDD | B-06223004250385 | Class IIa | Active |
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Manufacturer
- EUDAMED SRN
- EG-MF-000038562
- Authorised Representative
- Obelis s.a. BE-AR-000000106
Sources (2)
- EUDAMED e3252c2f-023e-44da-a9aa-13de0ccc6a4b 61 fields · synced Oct 7, 2026
- EUDAMED ad570b50-a8f2-40c8-9122-9fa146d0928c 61 fields · synced May 18, 2026