Identity
- Trade Name
- FUJIFILM FDA UDI
- Generic Name
- Luminal device flushing tubing set, reusable FDA UDI
- Device Name
- This product is the cleaning adapter used in combination with our endoscopes in medical facilities. Do not use this product for any other purpose. FDA UDI
- Model / Reference
- CA-500D/A FDA UDI
- Description
- This product is the cleaning adapter used in combination with our endoscopes in medical facilities. Do not use this product for any other purpose. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04547410111897 FDA UDI
- FDA Product Code
- FFY FDA UDI
- GMDN Term
- Luminal device flushing tubing set, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Luminal device flushing tubing set, reusable
Fujifilm by FUJIFILM Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Water-resistant cap — Olympus Medical Systems Corporation · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- FUJIFILM Corporation
Sources (1)
- FDA UDI c0234e7d-b84d-4641-be0b-314eedb9ce10 35 fields · synced May 31, 2026