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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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GTM SHOCK ABSORBER — 1 UDI-DI variant, MDD

MD Atlas
GTM-MOBIL M-T T.WALISIEWICZ SPÓŁKA KOMANDYTOWA

Data from EUDAMED, last updated May 31, 2026

GTM SHOCK ABSORBER

B-05904422167103

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class I

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Manufacturer: GTM-MOBIL M-T T.WALISIEWICZ SPÓŁKA KOMANDYTOWA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: B-05904422167103
Device name: GTM SHOCK ABSORBER
Device model: GTM SHOCK ABSORBER
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Version date: May 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: GTM-MOBIL M-T T.WALISIEWICZ SPÓŁKA KOMANDYTOWA
SRN: PL-MF-000035144
Country: Poland
Email: info@gtmmobil.com.pl
Phone: +48 22 213 14 11

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KSSR7M5GY1XGPMCNKHNHM3RB

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

01-001005904422167103