Identity
- Device Name
- Single Use Anoscope Kit EUDAMED
- Model / Reference
- AK30R EUDAMEDAK32B EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06971062270721 EUDAMED
- Basic UDI-DI
- 697106227AKWL EUDAMED
- EMDN Code
- G02060301 ANOSCOPES EUDAMED
Classification
- Device Class
- Class I 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
Single Use Anoscope Kit by Suzhou Lantex Medical Technology Company Limited — Class I — CE/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 | 697106227AKWL | Class I | Active |
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Manufacturer
- Manufacturer
- Suzhou Lantex Medical Technology Company Limited
- EUDAMED SRN
- CN-MF-000039444
- Authorised Representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Sources (1)
- EUDAMED c52ba99a-5720-4a7e-955a-df08e8be407a 61 fields · synced Oct 6, 2026