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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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BOWIE & DICK TEST PACK — 2 UDI-DI variants, MDR

MD Atlas
Akzenta International SA

Data from EUDAMED, last updated May 31, 2026

BOWIE & DICK TEST PACK

42504766BDDSG

2 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: Akzenta International SA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42504766BDDSG
Device name: BOWIE & DICK TEST PACK
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: Akzenta International SA
SRN: CH-MF-000036434
Country: Switzerland
Email: business@akzenta.ch
Phone: +41 (0) 91 921 14 92

Authorised representative

Name: IQX GmbH
SRN: AT-AR-000016713
Country: Austria
Phone: +4369919027671

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KSSAW257TM02825FFXA194NS

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

109101004250476600822
BDDAA26-AKZ-ST-UNI04250476600709