gudid
Primary ID: C2C12
GelPOINT V-Path (UDI C2C12)
Manufactured by APPLIED MEDICAL RESOURCES CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GelPOINT V-Path - Primary ID C2C12
Device Regulatory Overview
The GelPOINT V-Path (Model/Catalog Number: C2C12) is a medical device manufactured by APPLIED MEDICAL RESOURCES CORPORATION. This product is indexed under FDA Product Code / Category Classification MOK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- C2C12
- Product Code / EMDN
- MOK
- Device Name
- Transvaginal Access Platform with Total vNOTES Access System
- Database Sync Date
- 2026-08-09 09:31:01
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 GelPOINT V-Path?
The registered manufacturer of record for GelPOINT V-Path is APPLIED MEDICAL RESOURCES CORPORATION.
What is the Primary UDI-DI identifier for GelPOINT V-Path?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is C2C12.
What classification code is assigned to this device?
This device is registered under product classification code MOK.
Similar Classification Devices (MOK)
Other Devices by APPLIED MEDICAL RESOURCES CORPORATION
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