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MedK Hydrophilic Guidewires
EUDAMEDClass III (EU MDR)
Ref 98261SNC260HPC035Model MedK Hydrophilic Guidewires
by medK GmbH
Identity
- Device Name
- MedK Hydrophilic Guidewires EUDAMED
- Model / Reference
- MedK Hydrophilic Guidewires EUDAMED98261SNC260HPC035 EUDAMED
Identifiers
- Primary DI / UDI-DI
- +B82798261SNC260HPC0351 EUDAMED
- Basic UDI-DI
- ++B82798261LH EUDAMED
- EMDN Code
- C04030101 DIAGNOSTIC CORONARY AND PERIPHERAL VASCULAR GUIDE WIRES, HYDROPHILIC EUDAMED
Classification
- Device Class
- Class III EUDAMED
- Market of Registration
- Germany 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
MedK Hydrophilic Guidewires by medK GmbH — Class III — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | ++B82798261LH | Class III | Active |
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Manufacturer
- Manufacturer
- medK GmbH
- EUDAMED SRN
- DE-MF-000006273
Sources (1)
- EUDAMED 20382774-099d-4e03-847e-6768317412dc 61 fields · synced Aug 1, 2026