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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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Haltegriff 5179 — 10 UDI-DI variants, MDR (Meyra GmbH)

MD Atlas
Meyra GmbH

Data from EUDAMED, last updated May 23, 2026

Haltegriff 5179

4032766027907A

10 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: Meyra GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4032766027907A
Device name: Haltegriff 5179
Device model: Rehabilitation 5179
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: Meyra GmbH
SRN: DE-MF-000005780
Country: Germany
Email: info@meyra.de
Phone: +4957193292000

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01G3BM7PMHGW2BJAN9JCF9KJ88

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

29251201204032766027911
29251206204032766027966
29251203204032766027935
29251202204032766027928
29251207204032766027973
29251200204032766027904
29251208204032766027980
29251209204032766240792
29251205204032766027959
29251204204032766027942