GUDIDData
gudid Primary ID: BR70

Beurer (UDI BR70)

Manufactured by BEURER NORTH AMERICA, L.P.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Beurer - Primary ID BR70

Device Regulatory Overview

The Beurer (Model/Catalog Number: BR70) is a medical device manufactured by BEURER NORTH AMERICA, L.P.. This product is indexed under FDA Product Code / Category Classification IRT within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
BR70
Product Code / EMDN
IRT
Device Name
Insect Bite Healer
Database Sync Date
2026-08-09 09:12:32

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 Beurer?

The registered manufacturer of record for Beurer is BEURER NORTH AMERICA, L.P..

What is the Primary UDI-DI identifier for Beurer?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BR70.

What classification code is assigned to this device?

This device is registered under product classification code IRT.

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