Identity
- Trade Name
- VS3-NE FDA UDI
- Generic Name
- Endoscope video camera FDA UDI
- Device Name
- VS3 Endoscope 4mm, Elbow, 0°, Wide FOV FDA UDI
- Model / Reference
- 153-0006 FDA UDI
- Description
- VS3 Endoscope 4mm, Elbow, 0°, Wide FOV FDA UDI
Identifiers
- Catalog Number
- 153-0006 FDA UDI
- Primary DI / UDI-DI
- 18130400103397 FDA UDI
- 510(k) Number
- K131434 FDA UDI
- FDA Product Code
- GWG FDA UDI
- GMDN Term
- Endoscope video camera FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.1480 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-Ne by Visionsense Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K131434 also covers:
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 1cce1564-eb3c-4d21-930e-fdd9272392f6 36 fields · synced May 30, 2026