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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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babybay Medicare/Medicare Twins… — 4 UDI-DI variants, MDR

MD Atlas
Tobi GmbH & Co.KG

Data from EUDAMED, last updated May 23, 2026

babybay Medicare/Medicare Twins bedside sleeper

426009522babybay1501XXN6

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: Tobi GmbH & Co.KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426009522babybay1501XXN6
Device name: babybay Medicare/Medicare Twins bedside sleeper
Device model: babybay Medicare/Medicare Twins
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 11, 2026

Manufacturer & authorised representative

Manufacturer

Name: Tobi GmbH & Co.KG
SRN: DE-MF-000034484
Country: Germany
Email: s.graef@babybay.de

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K1ZRBN5GD9AW5ZC19FMGR012

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

15015204260472559260
15615104260095221186
15615204260472559383
15015104260095222220