eudamed_udi
Primary ID: 06951454729235
Plaster set (UDI 06951454729235)
Manufactured by GAUKE Healthcare Co., Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Plaster set - Primary ID 06951454729235
Device Regulatory Overview
The Plaster set (Model/Catalog Number: /) is a medical device manufactured by GAUKE Healthcare Co., Ltd. This product is indexed under FDA Product Code / Category Classification M03030202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- /
- Product Code / EMDN
- M03030202
- Device Name
- Adhesive bandage
- Database Sync Date
- 2026-08-09 16:46:26
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 Plaster set?
The registered manufacturer of record for Plaster set is GAUKE Healthcare Co., Ltd.
What is the Primary UDI-DI identifier for Plaster set?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06951454729235.
What classification code is assigned to this device?
This device is registered under product classification code M03030202.
Similar Classification Devices (M03030202)
Other Devices by GAUKE Healthcare Co., Ltd
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