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
π Token Gated
{
"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 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.
Similar Classification Devices (V080302)
Other Devices by Helping Hand Company (Ledbury) Ltd
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