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Channel Cleaning Adapter OF-B75
EUDAMEDFDA UDIClass I (EU MDR)
Ref 6217001Z970SModel See UDI-DI information for model names
Identity
- Trade Name
- Channel Cleaning Adapter OF-B75 EUDAMEDPENTAX FDA UDI
- Generic Name
- Endoscope leak tester tubing FDA UDI
- Device Name
- Channel Cleaning Adapter EUDAMEDSuction Channel Cleaning & Disinfection Adapter FDA UDI
- Model / Reference
- See UDI-DI information for model names EUDAMED6217001Z970S EUDAMEDOF-B75 FDA UDI
- Description
- Suction Channel Cleaning & Disinfection Adapter FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04961333073009 EUDAMEDFDA UDI
- Basic UDI-DI
- 4961333010509YG EUDAMED
- 510(k) Number
- K023376 FDA UDI
- FDA Product Code
- EOQ FDA UDI
- EMDN Code
- V0799 PRODUCTS FOR CLEANING MEDICAL DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
- GMDN Term
- Endoscope leak tester tubing FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 874.4680 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
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
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Channel Cleaning Adapter OF-B75 by HOYA Corporation — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 4961333010509YG | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- HOYA Corporation
- EUDAMED SRN
- JP-MF-000005227
- Authorised Representative
- PENTAX Europe GmbH DE-AR-000000006
Sources (2)
- EUDAMED 5a89ae46-2794-4165-bc8e-5b6d1f30c1f9 61 fields · synced Jun 19, 2026
- FDA UDI 0f851ce0-969b-45f1-9565-67bdb89f206c 34 fields · synced May 30, 2026