GUDIDData
eudamed_udi Primary ID: 05050962171169

HANDIGRIP PRO 31.5(80CM)YELLOW (UDI 05050962171169)

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 HANDIGRIP PRO 31.5(80CM)YELLOW - Primary ID 05050962171169

Device Regulatory Overview

The HANDIGRIP PRO 31.5(80CM)YELLOW (Model/Catalog Number: HA8232P) 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
HA8232P
Product Code / EMDN
Y242103
Device Name
TIDY JON 18IN (45CM) RED
Database Sync Date
2026-08-09 18:54:11

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 HANDIGRIP PRO 31.5(80CM)YELLOW?

The registered manufacturer of record for HANDIGRIP PRO 31.5(80CM)YELLOW is Helping Hand Company (Ledbury) Ltd.

What is the Primary UDI-DI identifier for HANDIGRIP PRO 31.5(80CM)YELLOW?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05050962171169.

What classification code is assigned to this device?

This device is registered under product classification code Y242103.

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