GelPOINT Path Transanal Access Platform (UDI CNO12)
Manufactured by APPLIED MEDICAL RESOURCES CORPORATION
Device Regulatory Overview
The GelPOINT Path Transanal Access Platform (Model/Catalog Number: CNO12) is a medical device manufactured by APPLIED MEDICAL RESOURCES CORPORATION. This product is indexed under FDA Product Code / Category Classification FER within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CNO12
- Product Code / EMDN
- FER
- Device Name
- Transanal Access Platform
- Database Sync Date
- 2026-08-09 09:57:14
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 Path Transanal Access Platform?
The registered manufacturer of record for GelPOINT Path Transanal Access Platform is APPLIED MEDICAL RESOURCES CORPORATION.
What is the Primary UDI-DI identifier for GelPOINT Path Transanal Access Platform?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CNO12.
What classification code is assigned to this device?
This device is registered under product classification code FER.
Similar Classification Devices (FER)
Other Devices by APPLIED MEDICAL RESOURCES CORPORATION
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