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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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PEMF Applicators — 5 UDI-DI variants, MDR (BEMER Int. AG)

MD Atlas
BEMER Int. AG

Data from EUDAMED, last updated May 30, 2026

PEMF Applicators

764016146PEMFD8

5 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: BEMER Int. AG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 764016146PEMFD8
Device name: PEMF Applicators
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 28, 2023

Manufacturer & authorised representative

Manufacturer

Name: BEMER Int. AG
SRN: LI-MF-000002555
Country: Liechtenstein
Email: regulatory@bemergroup.com

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GTBV86ES35NG4B5GYD309WCG

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

43440007640161460089
43430007640161460072
43410007640161460065
43420007640161460096
43400007640161460188