eudamed_udi
Primary ID: 06951454738459
Wound compress (UDI 06951454738459)
Manufactured by GAUKE Healthcare Co., Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Wound compress - Primary ID 06951454738459
Device Regulatory Overview
The Wound compress (Model/Catalog Number: 0501035) is a medical device manufactured by GAUKE Healthcare Co., Ltd. This product is indexed under FDA Product Code / Category Classification M040204 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0501035
- Product Code / EMDN
- M040204
- Device Name
- Absorbent non woven Compress
- Database Sync Date
- 2026-08-09 16:29:52
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 Wound compress?
The registered manufacturer of record for Wound compress is GAUKE Healthcare Co., Ltd.
What is the Primary UDI-DI identifier for Wound compress?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06951454738459.
What classification code is assigned to this device?
This device is registered under product classification code M040204.
Similar Classification Devices (M040204)
Other Devices by GAUKE Healthcare Co., Ltd
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