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PENTAX Medical Video Duodenoscope ED34-i10cT
EUDAMEDClass IIa (EU MDR)
Ref 6217001S339SModel See UDI-DI information for model names
Identity
- Trade Name
- PENTAX Medical Video Duodenoscope ED34-i10cT EUDAMED
- Device Name
- PENTAX Medical Video Duodenoscope EUDAMED
- Model / Reference
- See UDI-DI information for model names EUDAMED6217001S339S EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04961333252039 EUDAMED
- Basic UDI-DI
- 4961333010103XG EUDAMED
- Direct Marketing DI
- 04961333252015 EUDAMED
- EMDN Code
- Z12020510 VIDEO GASTRODUODENOSCOPES EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
Yes
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
PENTAX Medical Video Duodenoscope ED34-i10cT by Hoya Corporation — Class IIa — 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 | 4961333010103XG | Class IIa | Active |
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Manufacturer
- Manufacturer
- HOYA Corporation
- EUDAMED SRN
- JP-MF-000005227
- Authorised Representative
- PENTAX Europe GmbH DE-AR-000000006
Sources (1)
- EUDAMED 7c1a306c-1927-4f83-8e20-2ff13d8c3cdb 61 fields · synced May 23, 2026