eudamed_udi
Primary ID: 05050962253322
FOAM K YELLOW (UDI 05050962253322)
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 FOAM K YELLOW - Primary ID 05050962253322
Device Regulatory Overview
The FOAM K YELLOW (Model/Catalog Number: SA705) is a medical device manufactured by Helping Hand Company (Ledbury) Ltd. This product is indexed under FDA Product Code / Category Classification V080302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SA705
- Product Code / EMDN
- V080302
- Device Name
- SYMMETRISLEEP
- Database Sync Date
- 2026-08-09 17:08:19
Full Regulatory Attributes
π Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of FOAM K YELLOW?
The registered manufacturer of record for FOAM K YELLOW is Helping Hand Company (Ledbury) Ltd.
What is the Primary UDI-DI identifier for FOAM K YELLOW?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05050962253322.
What classification code is assigned to this device?
This device is registered under product classification code V080302.
Similar Classification Devices (V080302)
Other Devices by Helping Hand Company (Ledbury) Ltd
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint