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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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ErgoFlex — 6 UDI-DI variants, MDR (spektramed GmbH)

MD Atlas
spektramed GmbH

Data from EUDAMED, last updated May 23, 2026

ErgoFlex

425055662314022BS

6 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: spektramed GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 425055662314022BS
Device name: ErgoFlex
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 14, 2021

Manufacturer & authorised representative

Manufacturer

Name: spektramed GmbH
SRN: DE-MF-000005711
Country: Germany
Email: info@spektramed.de
Phone: +49243499334-0

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01FPJ415EN402TBGA85P919DHD

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

10002402304250556604757
10002402204250556604740
10002402104250556604733
10002402404250556604764
10002402504250556604771
10002402604250556604788