Identity
- Trade Name
- Via Procedure kit FDA UDI
- Generic Name
- Endoscopy preparation kit FDA UDI
- Device Name
- The VIA Procedure kit includes basin, sponge, gauze pads, Biohazard Sticker, transport pad and Double Header Cleaning Brush. FDA UDI
- Model / Reference
- 719706 FDA UDI
- Description
- The VIA Procedure kit includes basin, sponge, gauze pads, Biohazard Sticker, transport pad and Double Header Cleaning Brush. FDA UDI
Identifiers
- Catalog Number
- 00719706 FDA UDI
- Primary DI / UDI-DI
- 00816765013526 FDA UDI
- FDA Product Code
- NWU FDA UDI
- GMDN Term
- Endoscopy preparation kit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Via Procedure kit by US Endoscopy — 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- US Endoscopy
Sources (1)
- FDA UDI acc384fe-abf8-4201-922f-316985fcd4e7 36 fields · synced May 30, 2026