Identity
- Trade Name
- VIA FDA UDI
- Generic Name
- Endoscopy preparation kit FDA UDI
- Device Name
- The VIA procedure kit custom includes gauze, chux pad, basin, enzymatic sponge, lubricating jelly, suction tubing, BioGuard air water cleaning adapter, BioShield biopsy valve, and Torrent scope connector. FDA UDI
- Model / Reference
- 00717247 FDA UDI
- Description
- The VIA procedure kit custom includes gauze, chux pad, basin, enzymatic sponge, lubricating jelly, suction tubing, BioGuard air water cleaning adapter, BioShield biopsy valve, and Torrent scope connector. FDA UDI
Identifiers
- Catalog Number
- 00717247 FDA UDI
- Primary DI / UDI-DI
- 00816765016145 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 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 |
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Manufacturer
- Manufacturer
- US Endoscopy
Sources (1)
- FDA UDI f6036cdc-b0c5-4afe-ba75-1c6152573dde 36 fields · synced May 31, 2026