Identity
- Trade Name
- PENTAX FDA UDI
- Generic Name
- Flexible fibreoptic gastroscope FDA UDI
- Device Name
- GASTRO FIBERSCOPE FG-29V FDA UDI
- Model / Reference
- FG-29V FDA UDI
- Description
- GASTRO FIBERSCOPE FG-29V FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04961333228584 FDA UDI
- FDA Product Code
- FDS FDA UDI
- GMDN Term
- Flexible fibreoptic gastroscope FDA UDI
Classification
- Device Class
- Class II 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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Flexible fibreoptic gastroscope
Pentax by Hoya Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Flexible fibreoptic gastroscope.
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- MEDISONO — Medisono, LLC · Class II
- MEDISONO — Medisono, LLC · Class II
- MEDISONO — Medisono, LLC · Class II
- MEDISONO — Medisono, LLC · Class II
- MEDISONO — Medisono, LLC · Class II
- MEDISONO — Medisono, LLC · 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 II | Pending data |
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Manufacturer
- Manufacturer
- Hoya Corporation
Sources (1)
- FDA UDI a01d8820-ffb9-4b20-a6b3-094b3b26b2db 33 fields · synced May 30, 2026