Splint (UDI 06977728545240)
Manufactured by Suzhou Ireland Medical Equipment Co., Ltd.
Device Regulatory Overview
The Splint (Model/Catalog Number: DW-VS3) is a medical device manufactured by Suzhou Ireland Medical Equipment 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-VS3
- Product Code / EMDN
- M03050299
- Device Name
- Splint
- Database Sync Date
- 2026-08-09 16:48:03
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 Suzhou Ireland Medical Equipment Co., Ltd..
What is the Primary UDI-DI identifier for Splint?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06977728545240.
What classification code is assigned to this device?
This device is registered under product classification code M03050299.
Similar Classification Devices (M03050299)
Other Devices by Suzhou Ireland Medical Equipment Co., Ltd.
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