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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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BABIX — 2 UDI-DI variants, MDR (Hugo Rost & Co GmbH)

MD Atlas
Hugo Rost & Co GmbH

Data from EUDAMED, last updated May 23, 2026

BABIX

426247407BABIX42

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: Hugo Rost & Co GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426247407BABIX42
Device name: BABIX
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 22, 2024

Manufacturer & authorised representative

Manufacturer

Name: Hugo Rost & Co GmbH
SRN: DE-MF-000041490
Country: Germany
Email: info@hugo-rost.de

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HW2QEHAN2YWJ97A97RP9DB1N

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

BABIX U04262474070002
BABIX F04262474070019