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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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Careturner — 5 UDI-DI variants, MDR (Careturner A/S)

MD Atlas
Careturner A/S

Data from EUDAMED, last updated May 23, 2026

Careturner

5745000569CARETURNERBT

5 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: Careturner A/S

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UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01JF7Z4MQ5G1C5X1AHHNGPSDHR

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

CTUUNIVE30112205745000569120
CTUWIBOS31022505745000569151
ABLOPU1731022505745000569168
CTUWIBMUL32032605745000569182
IVCSB7NO31022505745000569175

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5745000569CARETURNERBT
Device name: Careturner
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 16, 2024

Manufacturer & authorised representative

Manufacturer

Name: Careturner A/S
SRN: DK-MF-000020149
Country: Denmark
Email: info@careturner.com
Phone: 20978115

Variants by status