eudamed_udi
Primary ID: 06974679018861
Splint (UDI 06974679018861)
Manufactured by Dragon Medical Co.,Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Splint - Primary ID 06974679018861
Device Regulatory Overview
The Splint (Model/Catalog Number: DW-FT08) is a medical device manufactured by Dragon Medical 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
- DW-FT08
- Product Code / EMDN
- M03050299
- Device Name
- Splint
- Database Sync Date
- 2026-08-09 16:28:55
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?
The registered manufacturer of record for Splint is Dragon Medical Co.,Ltd.
What is the Primary UDI-DI identifier for Splint?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974679018861.
What classification code is assigned to this device?
This device is registered under product classification code M03050299.
Similar Classification Devices (M03050299)
Other Devices by Dragon Medical Co.,Ltd
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