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, biohazard sticker, VIA basin, enzymatic sponge, lubricating jelly, suction tubing, syringe, BioGuard 4-piece kit, and BioGuard air water cleaning adapter. FDA UDI
- Model / Reference
- 00717215 FDA UDI
- Description
- The VIA procedure kit custom includes transport pad, gauze pads, biohazard sticker, VIA basin, enzymatic sponge, lubricating jelly, suction tubing, syringe, BioGuard 4-piece kit, and BioGuard air water cleaning adapter. FDA UDI
Identifiers
- Catalog Number
- 00717215 FDA UDI
- Primary DI / UDI-DI
- 00816765015872 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
Yes
FDA UDI
A comprehensive procedure kit designed for endoscopic procedures, including gastrointestinal and urological procedures. The kit includes a variety of tools and supplies to support the procedure.
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 b220a80b-babd-4b32-890f-b548b1e406ae 36 fields · synced Jul 15, 2026