Identity
- Trade Name
- ViaLens Patient Interface EUDAMED
- Device Name
- ViaLens Patient Interface EUDAMED
- Model / Reference
- 101-0005 EUDAMED
Identifiers
- Primary DI / UDI-DI
- +G13010100050P EUDAMED
- Basic UDI-DI
- ++G1301010005GD EUDAMED
- EMDN Code
- Z12011085 LASER SURGERY INSTRUMENTS - CONSUMABLES EUDAMED
Classification
- Device Class
- Class IIa 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
Category: Varicose vein lasing procedure kit
ViaLens Patient Interface by ViaLase, Inc. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS
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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 | ++G1301010005GD | Class IIa | Active |
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Manufacturer
- Manufacturer
- ViaLase, Inc.
- EUDAMED SRN
- US-MF-000018934
- Authorised Representative
- MDSS GmbH DE-AR-000005430
Sources (1)
- EUDAMED a0f6f22a-22ba-4bb2-901e-f343db7704a3 61 fields · synced Jul 8, 2026