Spine board (UDI 06977728542676)
Manufactured by Suzhou Ireland Medical Equipment Co., Ltd.
Device Regulatory Overview
The Spine board (Model/Catalog Number: DW-PE004) is a medical device manufactured by Suzhou Ireland Medical Equipment Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Y060312 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DW-PE004
- Product Code / EMDN
- Y060312
- Device Name
- Spine board
- Database Sync Date
- 2026-08-09 16:30:15
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 Spine board?
The registered manufacturer of record for Spine board is Suzhou Ireland Medical Equipment Co., Ltd..
What is the Primary UDI-DI identifier for Spine board?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06977728542676.
What classification code is assigned to this device?
This device is registered under product classification code Y060312.
Similar Classification Devices (Y060312)
Other Devices by Suzhou Ireland Medical Equipment Co., Ltd.
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