gudid
Primary ID: VIA Custom Procedure Kit
VIA (UDI VIA Custom Procedure Kit)
Manufactured by US Endoscopy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VIA - Primary ID VIA Custom Procedure Kit
Device Regulatory Overview
The VIA (Model/Catalog Number: VIA Custom Procedure Kit) is a medical device manufactured by US Endoscopy. This product is indexed under FDA Product Code / Category Classification NWU within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- VIA Custom Procedure Kit
- Product Code / EMDN
- NWU
- Device Name
- The VIA Procedure Kit - custom includes Enzymatic Sponge, Tray, Olympus 4-piece Valve Kit, BioShield Biopsy Valve, Absorbent Pad, Lubricant, Gauze, Simethicone Water Label, and Biohazard Sticker.
- Database Sync Date
- 2026-08-09 09:19:08
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of VIA?
The registered manufacturer of record for VIA is US Endoscopy.
What is the Primary UDI-DI identifier for VIA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VIA Custom Procedure Kit.
What classification code is assigned to this device?
This device is registered under product classification code NWU.
Similar Classification Devices (NWU)
Other Devices by US Endoscopy
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