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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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Contact Shock Freezer — 6 UDI-DI variants, MDR

MD Atlas
B Medical Systems S.à r.l.

Data from EUDAMED, last updated May 30, 2026

Contact Shock Freezer

05450104511103A8

6 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: B Medical Systems S.à r.l.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 05450104511103A8
Device name: Contact Shock Freezer
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: B Medical Systems S.à r.l.
SRN: LU-MF-000000128
Country: Luxembourg
Email: annika.hartmann@bmedicalsystems.com
Phone: +352 920731386

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G3R0X04TE3SCQKXJ11SK538Z

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

991.9000.**05450104537936
991.9020.**05450104540899
991.9010.**05450104540882
991.8900.**05450104537912
991.8920.**05450104540875
991.8910.**05450104540868