GUDIDData
eudamed_udi Primary ID: 07640161461017

BEMER Classic-Set (UDI 07640161461017)

Manufactured by BEMER Int. AG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BEMER Classic-Set - Primary ID 07640161461017

Device Regulatory Overview

The BEMER Classic-Set (Model/Catalog Number: 410100) is a medical device manufactured by BEMER Int. AG. This product is indexed under FDA Product Code / Category Classification Z12062801 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
410100
Product Code / EMDN
Z12062801
Device Name
BEMER Classic-Set
Database Sync Date
2026-08-09 17:12:15

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 BEMER Classic-Set?

The registered manufacturer of record for BEMER Classic-Set is BEMER Int. AG.

What is the Primary UDI-DI identifier for BEMER Classic-Set?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07640161461017.

What classification code is assigned to this device?

This device is registered under product classification code Z12062801.

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