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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 střední riziko… — 8 UDI-DI variants, MDR

MD Atlas
LB BOHEMIA, s.r.o.

Data from EUDAMED, last updated May 23, 2026

Matrace Bohemia pro střední riziko vzniku dekubitů

08595193700209V8

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: 08595193700209V8
Device name: Matrace Bohemia pro střední 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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Applied filters

basicUdiUlid01KM0KCM5ZF12EB6NJNJK0FF8S

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/A08595193700223
N/A08595193700247
N/A08595193700230
N/A08595193701107
N/A08595193700261
N/A08595193700278
N/A08595193700254
N/A08595193701114