GUDIDData
eudamed_udi Primary ID: 05050962088412

FA2014 (UDI 05050962088412)

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 FA2014 - Primary ID 05050962088412

Device Regulatory Overview

The FA2014 (Model/Catalog Number: FA2014) 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
FA2014
Product Code / EMDN
V080302
Device Name
SYMMKIT ACHEEVA JNR STARTER SUPPORT PACK
Database Sync Date
2026-08-09 17:33:24

Full Regulatory Attributes

πŸ”’ 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 FA2014?

The registered manufacturer of record for FA2014 is Helping Hand Company (Ledbury) Ltd.

What is the Primary UDI-DI identifier for FA2014?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05050962088412.

What classification code is assigned to this device?

This device is registered under product classification code V080302.

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