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Via

FDA UDI

Class II (US FDA UDI)

by US Endoscopy

Identity

Trade Name
VIA FDA UDI
Generic Name
Endoscopy preparation kit FDA UDI
Device Name
The VIA Procedure Kit-custom includes transport pad, gauze, Via Basin, lubrication jelly, and BioGuard 4-piece kit. FDA UDI
Model / Reference
00717186 FDA UDI
Description
The VIA Procedure Kit-custom includes transport pad, gauze, Via Basin, lubrication jelly, and BioGuard 4-piece kit. FDA UDI

Identifiers

Catalog Number
00717186 FDA UDI
Primary DI / UDI-DI
00724995183295 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
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

Category: Endoscopy preparation kit

Via by US Endoscopy — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopy preparation kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
US Endoscopy

Sources (1)

  • FDA UDI bf037f11-7ad3-41f1-9db5-47741e87d2f3 35 fields · synced May 31, 2026