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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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Halteband — 5 UDI-DI variants, MDR

MD Atlas
GERWING Medizinprodukte Gerd Riester e.K.

Data from EUDAMED, last updated May 23, 2026

Halteband

426046972GE067E

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: GERWING Medizinprodukte Gerd Riester e.K.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426046972GE067E
Device name: Halteband
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 26, 2022

Manufacturer & authorised representative

Manufacturer

Name: GERWING Medizinprodukte Gerd Riester e.K.
SRN: DE-MF-000006156
Country: Germany
Email: info@gerwing-riester.de
Phone: +49 7477 152385

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01FTBG3ZN2JQHVG9Q8HEFSS8S5

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

GE 06-110104260469721083
GE 06-100104260469720789
GE 06-110204260469721090
GE 06-100204260469720796
GE 06-100304260469720802