eudamed_udi
Primary ID: 05050962437616
SLING (UDI 05050962437616)
Manufactured by Helping Hand Company (Ledbury) Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SLING - Primary ID 05050962437616
Device Regulatory Overview
The SLING (Model/Catalog Number: RDIBES5XBAB) is a medical device manufactured by Helping Hand Company (Ledbury) Ltd. This product is indexed under FDA Product Code / Category Classification V0805038002 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RDIBES5XBAB
- Product Code / EMDN
- V0805038002
- Device Name
- SLINGS
- Database Sync Date
- 2026-08-09 16:45:55
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 SLING?
The registered manufacturer of record for SLING is Helping Hand Company (Ledbury) Ltd.
What is the Primary UDI-DI identifier for SLING?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05050962437616.
What classification code is assigned to this device?
This device is registered under product classification code V0805038002.
Similar Classification Devices (V0805038002)
Other Devices by Helping Hand Company (Ledbury) Ltd
Programmatic Export
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