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ULTRAMED A.V. FISTULA NEEDLE 17 G (Double)
EUDAMEDClass IIa (EU MDR)
Ref 9003-17/DModel ULTRAMED A.V. FISTULA NEEDLE 17 G (Double)Model ULTRAMED A.V. FISTULA NEEDLE
Identity
- Trade Name
- ULTRAMED A.V. FISTULA NEEDLE 17 G (Double) EUDAMED
- Device Name
- ULTRAMED A.V. FISTULA NEEDLE EUDAMED
- Model / Reference
- ULTRAMED A.V. FISTULA NEEDLE 17 G (Double) EUDAMED9003-17/D EUDAMEDULTRAMED A.V. FISTULA NEEDLE EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06223004254130 EUDAMED
- Basic UDI-DI
- B-06223004254130 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 (Double) by Ultra For Medical Products (Ultramed) U.M.I.C (S.A.E) — Class IIa — MDD, MDR — listed in EUDAMED
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-06223004254130 | Class IIa | Active |
| EUDAMED | European Union | CE/MDR | B-06223004254130 | Class IIa | Active |
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Manufacturer
- EUDAMED SRN
- EG-MF-000038562
- Authorised Representative
- Obelis s.a. BE-AR-000000106
Sources (2)
- EUDAMED 037e34cf-c023-4b50-8023-d6436bb4ce8c 61 fields · synced Oct 6, 2026
- EUDAMED 3c47641f-35fd-4356-b4ee-8c5f6f635018 61 fields · synced May 17, 2026