Identity
- Trade Name
- VS3-IR FDA UDI
- Generic Name
- Endoscope video camera FDA UDI
- Device Name
- VS3 Iridium Endoscope-IR 5.5mm, Long, 0°, Standard FOV - Refurbished FDA UDI
- Model / Reference
- 153-0051RFB FDA UDI
- Description
- VS3 Iridium Endoscope-IR 5.5mm, Long, 0°, Standard FOV - Refurbished FDA UDI
Identifiers
- Catalog Number
- 153-0051RFB FDA UDI
- Primary DI / UDI-DI
- 10813040013247 FDA UDI
- FDA Product Code
- GWG FDA UDIOWN FDA UDIGCJ FDA UDIHRX FDA UDI
- GMDN Term
- Endoscope video camera FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.1480 FDA UDI876.1500 FDA UDI888.1100 FDA UDI
- Commercial Distribution
- Not 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
No
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
Vs3-Ir by Visionsense Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Visionsense Ltd.
Sources (1)
- FDA UDI f2084b14-8c2b-4aac-816d-3161e1a1229d 35 fields · synced Jun 8, 2026