gudid
Primary ID: C1
cofoe (UDI C1)
Manufactured by Cofoe Medical Technology Co.,Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for cofoe - Primary ID C1
Device Regulatory Overview
The cofoe (Model/Catalog Number: C1) is a medical device manufactured by Cofoe Medical Technology Co.,Ltd. This product is indexed under FDA Product Code / Category Classification EXE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- C1
- Product Code / EMDN
- EXE
- Device Name
- Skin Barrier Wipe
- Database Sync Date
- 2026-08-09 09:05:26
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 cofoe?
The registered manufacturer of record for cofoe is Cofoe Medical Technology Co.,Ltd.
What is the Primary UDI-DI identifier for cofoe?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is C1.
What classification code is assigned to this device?
This device is registered under product classification code EXE.
Similar Classification Devices (EXE)
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