gudid
Primary ID: V618
Vilet (UDI V618)
Manufactured by RIVERPOINT MEDICAL, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vilet - Primary ID V618
Device Regulatory Overview
The Vilet (Model/Catalog Number: V618) is a medical device manufactured by RIVERPOINT MEDICAL, LLC. This product is indexed under FDA Product Code / Category Classification GAM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- V618
- Product Code / EMDN
- GAM
- Device Name
- Polyglactin 910 Violet Braided Suture
- Database Sync Date
- 2026-08-09 09:12:05
Full Regulatory Attributes
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{
"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 Vilet?
The registered manufacturer of record for Vilet is RIVERPOINT MEDICAL, LLC.
What is the Primary UDI-DI identifier for Vilet?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is V618.
What classification code is assigned to this device?
This device is registered under product classification code GAM.
Similar Classification Devices (GAM)
Other Devices by RIVERPOINT MEDICAL, LLC
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