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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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3-Kammer Kompressionsmanschetten — 4 UDI-DI variants, MDR

MD Atlas
BÖSL Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

3-Kammer Kompressionsmanschetten

426067522Z120607B03KM005D

4 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: BÖSL Medizintechnik GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426067522Z120607B03KM005D
Device name: 3-Kammer Kompressionsmanschetten
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 2025

Manufacturer & authorised representative

Manufacturer

Name: BÖSL Medizintechnik GmbH
SRN: DE-MF-000005321
Country: Germany
Email: info@boesl-med.de
Phone: +49 2405-69390-0

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JW5Z7Y3FH6KDEK230WB48VA5

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

35004260675220349
34004260675220332
33004260675220325
36004260675220356