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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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CareTainer — 8 UDI-DI variants, MDR (Omni-Pac GmbH Verpackungsmittel)

MD Atlas
Omni-Pac GmbH Verpackungsmittel

Data from EUDAMED, last updated May 23, 2026

CareTainer

426067659001BT

8 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: Omni-Pac GmbH Verpackungsmittel

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426067659001BT
Device name: CareTainer
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 18, 2025

Manufacturer & authorised representative

Manufacturer

Name: Omni-Pac GmbH Verpackungsmittel
SRN: DE-MF-000006833
Country: Germany
Email: info@omnipacgroup.com
Phone: +49 4404 9250

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01JZX02WXPN2KEG8Z43F3JCQEM

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

Omni Pac04260676590069
Omni Pac04260676590021
Omni Pac04260676590014
Omni Pac04260676590038
Omni Pac04260676590045
Omni Pac04260676590052
Omni Pac04260676590090
Omni Pac04260676590076