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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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BRUMABA Caddy — 4 UDI-DI variants, MDR (BRUMABA GmbH)

MD Atlas
BRUMABA GmbH

Data from EUDAMED, last updated May 23, 2026

BRUMABA Caddy

42602477718-139DY

4 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: BRUMABA GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 42602477718-139DY
Device name: BRUMABA Caddy
Device model: BRUMABA Caddy
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 17, 2023

Manufacturer & authorised representative

Manufacturer

Name: BRUMABA GmbH
SRN: DE-MF-000006236
Country: Germany
Email: info@brumaba.de
Phone: +49 (0) 8171 / 2672 – 0

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H0MC30FDNCXQC52KZ953GXQH

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

C1.02.1304260247770081
C1.01.1304260247770104
C1.02.0004260247770098
C1.01.0004260247770111