Identity
- Trade Name
- Peripheral Guidewires EUDAMED
- Device Name
- Guidewires EUDAMED
- Model / Reference
- 105235082 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 20886333000948 EUDAMED
- Basic UDI-DI
- B-20886333000948 EUDAMED
- EMDN Code
- A060299,C04020102 EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Netherlands 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
Peripheral Guidewires by Argon Medical Devices, 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-20886333000948 | Class IIa | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Argon Medical Devices, Inc.
- EUDAMED SRN
- US-MF-000002324
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (1)
- EUDAMED 285e2499-12fe-46b8-9820-7898c309eb88 61 fields · synced Jul 9, 2026