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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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Formidabel / FMB care elektrische… — 5 UDI-DI variants, MDR

MD Atlas
FMB Care GmbH

Data from EUDAMED, last updated May 23, 2026

Formidabel / FMB care elektrische Pflegebetten

PP10364CAREBED03

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: FMB Care GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: PP10364CAREBED03
Device name: Formidabel / FMB care elektrische Pflegebetten
Device model: Elektrische Pflegebetten
Issuing agency: IFA
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 30, 2026

Manufacturer & authorised representative

Manufacturer

Name: FMB Care GmbH
SRN: DE-MF-000005985
Country: Germany
Email: info@fmb-care.de

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQCR1KZ9MWC44SK7Q7AEA32Y

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

7000-xx-xx /_Eco111683107452
7000-xx-xx /_First111683104533
7000-xx-xx / Pro111683105196
7000-xx-xx / Pro+112015563888
7000-xx-xx /_UltraLow111662724469