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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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Careline — 20 UDI-DI variants, MDR (Greiner GmbH)

MD Atlas
Greiner GmbH

Data from EUDAMED, last updated May 23, 2026

Careline

406609844678

20 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: Greiner GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 406609844678
Device name: Careline
Device model: 446
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 8, 2022

Manufacturer & authorised representative

Manufacturer

Name: Greiner GmbH
SRN: DE-MF-000007660
Country: Germany
Email: thomas.wegmann@greiner-gmbh.de
Phone: 07144/811241

Variants by status

UDI-DI variants

20 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G9YW21HJH6H92PN38SWQEYHJ

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

446011004066098446027
447024104066098446195
447022104066098446188
446014004066098446089
446013004066098446065
446012004066098446041
446012104066098446058
446013104066098446072
446014104066098446096
446011104066098446034
446023004066098446140
446021004066098446102
446024004066098446164
446022004066098446126
446021104066098446119
446023104066098446157
446024104066098446171
446022104066098446133
944613704066098446782
446X00104066098446010