Identity
- Trade Name
- VIA FDA UDI
- Generic Name
- Endoscopy preparation kit FDA UDI
- Device Name
- The VIA procedure kit-custom includes transport pad, gauze pads, basin, enzymatic sponge, syringe, biohazard sticker, lubricating jelly, gown, DuoSwift combination squeegee brush, and BioGuard air water and suction valves 4 piece kit. FDA UDI
- Model / Reference
- 00717113 FDA UDI
- Description
- The VIA procedure kit-custom includes transport pad, gauze pads, basin, enzymatic sponge, syringe, biohazard sticker, lubricating jelly, gown, DuoSwift combination squeegee brush, and BioGuard air water and suction valves 4 piece kit. FDA UDI
Identifiers
- Catalog Number
- 00717113 FDA UDI
- Primary DI / UDI-DI
- 00816765015018 FDA UDI
- FDA Product Code
- NWW FDA UDI
- GMDN Term
- Endoscopy preparation kit FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 884.1690 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 I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- US Endoscopy
Sources (1)
- FDA UDI 40ea6c13-2482-4857-b178-d82383a6f66f 36 fields · synced May 31, 2026