eudamed_udi
Primary ID: 05740008104380
Winncare (UDI 05740008104380)
Manufactured by Winncare Nordic
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Winncare - Primary ID 05740008104380
Device Regulatory Overview
The Winncare (Model/Catalog Number: 083-10030EU) is a medical device manufactured by Winncare Nordic. This product is indexed under FDA Product Code / Category Classification V08050302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 083-10030EU
- Product Code / EMDN
- V08050302
- Device Name
- Ceiling Hoist
- Database Sync Date
- 2026-08-09 16:45:07
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 Winncare?
The registered manufacturer of record for Winncare is Winncare Nordic.
What is the Primary UDI-DI identifier for Winncare?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05740008104380.
What classification code is assigned to this device?
This device is registered under product classification code V08050302.
Similar Classification Devices (V08050302)
Other Devices by Winncare Nordic
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