eudamed_udi
Primary ID: 05050962369924
EQUASEAT MEDIUM (UDI 05050962369924)
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 EQUASEAT MEDIUM - Primary ID 05050962369924
Device Regulatory Overview
The EQUASEAT MEDIUM (Model/Catalog Number: PEQSIM) is a medical device manufactured by Helping Hand Company (Ledbury) Ltd. This product is indexed under FDA Product Code / Category Classification V080399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PEQSIM
- Product Code / EMDN
- V080399
- Device Name
- MEDIUM EQUAZONE CUSHION
- Database Sync Date
- 2026-08-09 16:28:44
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 EQUASEAT MEDIUM?
The registered manufacturer of record for EQUASEAT MEDIUM is Helping Hand Company (Ledbury) Ltd.
What is the Primary UDI-DI identifier for EQUASEAT MEDIUM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05050962369924.
What classification code is assigned to this device?
This device is registered under product classification code V080399.
Similar Classification Devices (V080399)
Other Devices by Helping Hand Company (Ledbury) Ltd
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