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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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Elbacare — 3 UDI-DI variants, MDR (tecfor care GmbH)

MD Atlas
tecfor care GmbH

Data from EUDAMED, last updated May 23, 2026

Elbacare

4068429Elbacare-36

3 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: tecfor care GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 4068429Elbacare-36
Device name: Elbacare
Device model: Electric medical bed
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 6, 2026

Manufacturer & authorised representative

Manufacturer

Name: tecfor care GmbH
SRN: DE-MF-000007722
Country: Germany
Email: info@tecfor-care.com
Phone: +49 (0) 2261 - 50186 - 0

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQYMNS7BFCTPFWKEY5QEESPY

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

0080004068429008003
0080604068429008065
0431704068429043172