GUDIDData
gudid Primary ID: 01

BestMove (UDI 01)

Manufactured by BESTCARE, L.L.C.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BestMove - Primary ID 01

Device Regulatory Overview

The BestMove (Model/Catalog Number: 01) is a medical device manufactured by BESTCARE, L.L.C.. This product is indexed under FDA Product Code / Category Classification FMR within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
01
Product Code / EMDN
FMR
Device Name
Bestcare BestMove STA400, 400lb, Manual, Red and White, MC
Database Sync Date
2026-08-09 09:06:21

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 BestMove?

The registered manufacturer of record for BestMove is BESTCARE, L.L.C..

What is the Primary UDI-DI identifier for BestMove?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 01.

What classification code is assigned to this device?

This device is registered under product classification code FMR.

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