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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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Mobile Blood Collection Bed — 9 UDI-DI variants, MDR (STRUB GMBH)

MD Atlas
STRUB GMBH

Data from EUDAMED, last updated May 23, 2026

Mobile Blood Collection Bed

42519192-MOB-BED87

9 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: STRUB GMBH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42519192-MOB-BED87
Device name: Mobile Blood Collection Bed
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 6, 2026

Manufacturer & authorised representative

Manufacturer

Name: STRUB GMBH
SRN: DE-MF-000034376
Country: Germany
Email: contact@strub-group.com
Phone: +49 6349928637

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01KE9CVKW58R1BZQGX39C45XHG

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

EM00-7302-STD-K0304251919200432
EM00-8002-C03-K0404251919200449
EM00-7302-STD-K0104251919200425
EM00-7302-C04-K0204251919200418
EU00-7312-C02-K0404251919200524
EU00-6612-C01-K0504251919200456
EU00-7312-STD-K0104251919200463
EU00-8012-STD-K0304251919200487
EU00-7312-STD-K0204251919200470