Stretcher (UDI 06977728544380)
Manufactured by Suzhou Ireland Medical Equipment Co., Ltd.
Device Regulatory Overview
The Stretcher (Model/Catalog Number: DW-FA009) is a medical device manufactured by Suzhou Ireland Medical Equipment Co., Ltd.. This product is indexed under FDA Product Code / Category Classification V08050103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DW-FA009
- Product Code / EMDN
- V08050103
- Device Name
- Stretcher
- Database Sync Date
- 2026-08-09 16:29:12
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 Stretcher?
The registered manufacturer of record for Stretcher is Suzhou Ireland Medical Equipment Co., Ltd..
What is the Primary UDI-DI identifier for Stretcher?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06977728544380.
What classification code is assigned to this device?
This device is registered under product classification code V08050103.
Similar Classification Devices (V08050103)
Other Devices by Suzhou Ireland Medical Equipment Co., Ltd.
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