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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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Dental Treatment Light — 2 UDI-DI variants, MDR (BPR Swiss GmbH)

MD Atlas
BPR Swiss GmbH

Data from EUDAMED, last updated May 23, 2026

Dental Treatment Light

76401850200003LW

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: BPR Swiss GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 76401850200003LW
Device name: Dental Treatment Light
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 29, 2025

Manufacturer & authorised representative

Manufacturer

Name: BPR Swiss GmbH
SRN: CH-MF-000018810
Country: Switzerland
Email: info@bpr-swiss.com
Phone: +41 31 506 06 06

Authorised representative

Name: Klaus Seiler
SRN: DE-AR-000016462
Country: Germany
Phone: +49 7551 949 7850

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01K1B6FX9PZKR8FHGQZZ1A032T

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

Denta-LED07640185020191
Sun-LED07640185020184