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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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B.Light — 1 UDI-DI variant, MDD (BEMER Int. AG)

MD Atlas
BEMER Int. AG

Data from EUDAMED, last updated May 30, 2026

B.Light

B-07640161460324

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIa

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: BEMER Int. AG

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Device characteristics

Active device

Legacy certificates

Certificate number: D1304700010
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: mdc medical device certification GmbH (0483)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-07640161460324
Device name: B.Light
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC 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

1 UDI-DI variant

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Applied filters

basicUdiUlid01GT9SRRPJ324C59017YQ08WHA

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

43120007640161460324