gudid
Primary ID: PU2
cofoe (UDI PU2)
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 PU2
Device Regulatory Overview
The cofoe (Model/Catalog Number: PU2) is a medical device manufactured by Cofoe Medical Technology Co.,Ltd. This product is indexed under FDA Product Code / Category Classification EZR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PU2
- Product Code / EMDN
- EZR
- Device Name
- Ostomy Barrier Strip
- 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 PU2.
What classification code is assigned to this device?
This device is registered under product classification code EZR.
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