eudamed_udi
Primary ID: 06951454727521
Splint Roll (UDI 06951454727521)
Manufactured by GAUKE Healthcare Co., Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Splint Roll - Primary ID 06951454727521
Device Regulatory Overview
The Splint Roll (Model/Catalog Number: 2301001) is a medical device manufactured by GAUKE Healthcare Co., Ltd. This product is indexed under FDA Product Code / Category Classification M03050299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2301001
- Product Code / EMDN
- M03050299
- Device Name
- First Aid Splint Roll
- Database Sync Date
- 2026-08-09 16:46:15
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 Splint Roll?
The registered manufacturer of record for Splint Roll is GAUKE Healthcare Co., Ltd.
What is the Primary UDI-DI identifier for Splint Roll?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06951454727521.
What classification code is assigned to this device?
This device is registered under product classification code M03050299.
Similar Classification Devices (M03050299)
Other Devices by GAUKE Healthcare Co., Ltd
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