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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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redconnect. Fahrtragenadapter — 4 UDI-DI variants, MDR (hestomed GmbH)

MD Atlas
hestomed GmbH

Data from EUDAMED, last updated May 23, 2026

redconnect. Fahrtragenadapter

426066638redconnectNP

4 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: hestomed GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426066638redconnectNP
Device name: redconnect. Fahrtragenadapter
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: hestomed GmbH
SRN: DE-MF-000006850
Country: Germany
Email: f.wagner@hestomed.de
Phone: 03720463818

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KFJFZ6TH2AQAG4QWD3QBTCBN

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

redconnect. adapter CPS04260666389765
redconnect. adapter Power X04260666389352
redconnect. adapter PowerPro XT04260666389772
redconnect. adapter PowerPro XT/204260666389840