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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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GD - Device Carriers — 6 UDI-DI variants, MDR (MAVIG GmbH)

MD Atlas
MAVIG GmbH

Data from EUDAMED, last updated May 23, 2026

GD - Device Carriers

4251339906310WF

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: MAVIG GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4251339906310WF
Device name: GD - Device Carriers
Device model: GD
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 19, 2024

Manufacturer & authorised representative

Manufacturer

Name: MAVIG GmbH
SRN: DE-MF-000006207
Country: Germany
Email: info@mavig.com
Phone: +49 89 42096 0

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01J5NB80N0F8E30VWS5HRE7HEP

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

GD60 Extension Spring Arm04251339906365
GD60 Extension Spring Arm04251339906334
GD60 Extension Spring Arm04251339906341
GD60 Extension Spring Arm04251339906358
GD60 Extension Spring Arm04251339906327
GD60SX0008-DR04251339906372