GUDIDData
eudamed_udi Primary ID: 05050962203983

ARTHRI GRIP PRO 81CM (32IN) (UDI 05050962203983)

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 ARTHRI GRIP PRO 81CM (32IN) - Primary ID 05050962203983

Device Regulatory Overview

The ARTHRI GRIP PRO 81CM (32IN) (Model/Catalog Number: HA8432P) is a medical device manufactured by Helping Hand Company (Ledbury) Ltd. This product is indexed under FDA Product Code / Category Classification Y242103 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
HA8432P
Product Code / EMDN
Y242103
Device Name
TIDY JON 18IN (45CM) RED
Database Sync Date
2026-08-09 16:29:04

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of ARTHRI GRIP PRO 81CM (32IN)?

The registered manufacturer of record for ARTHRI GRIP PRO 81CM (32IN) is Helping Hand Company (Ledbury) Ltd.

What is the Primary UDI-DI identifier for ARTHRI GRIP PRO 81CM (32IN)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05050962203983.

What classification code is assigned to this device?

This device is registered under product classification code Y242103.

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