eudamed_udi
Primary ID: 06950715573914
Alcohol Wipe (UDI 06950715573914)
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 Alcohol Wipe - Primary ID 06950715573914
Device Regulatory Overview
The Alcohol Wipe (Model/Catalog Number: 3cm×6cm) is a medical device manufactured by Cofoe Medical Technology Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification M02030202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3cm×6cm
- Product Code / EMDN
- M02030202
- Device Name
- Alcohol Wipe酒精棉片
- Database Sync Date
- 2026-08-09 16:58:48
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 Alcohol Wipe?
The registered manufacturer of record for Alcohol Wipe is Cofoe Medical Technology Co.,Ltd..
What is the Primary UDI-DI identifier for Alcohol Wipe?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06950715573914.
What classification code is assigned to this device?
This device is registered under product classification code M02030202.
Similar Classification Devices (M02030202)
Other Devices by Cofoe Medical Technology Co.,Ltd.
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