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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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Matrace Bohemia pro velmi vysoké… — 8 UDI-DI variants, MDR

MD Atlas
LB BOHEMIA, s.r.o.

Data from EUDAMED, last updated May 23, 2026

Matrace Bohemia pro velmi vysoké riziko vzniku dekubitů

08595193700223V2

8 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: LB BOHEMIA, s.r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 08595193700223V2
Device name: Matrace Bohemia pro velmi vysoké riziko vzniku dekubitů
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: LB BOHEMIA, s.r.o.
SRN: CZ-MF-000051784
Country: Czechia
Email: objednavky@LBBohemia.cz
Phone: +420 777 092 992

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KM0KCP4PN84JR3TXYN3NVGY5

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

N/A08595193700407
N/A08595193700414
N/A08595193700360
N/A08595193700353
N/A08595193700377
N/A08595193701138
N/A08595193700445
N/A08595193700452