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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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STARK STABILIZER Kołnierz sztywny z… — 13 UDI-DI variants, MDR

MD Atlas
mdh sp. z o. o.

Data from EUDAMED, last updated May 30, 2026

STARK STABILIZER Kołnierz sztywny z ortezą półgorsetową piersiową

59017804MQA2DSL7

13 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: mdh sp. z o. o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 59017804MQA2DSL7
Device name: STARK STABILIZER Kołnierz sztywny z ortezą półgorsetową piersiową
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 9, 2026

Manufacturer & authorised representative

Manufacturer

Name: mdh sp. z o. o.
SRN: PL-MF-000011406
Country: Poland
Email: biuro@mdh.pl

Variants by status

UDI-DI variants

13 UDI-DI variants

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Applied filters

basicUdiUlid01KH0NZ16WP2SVM9FE6ZZQ2J3Y

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

MQA2DSLAX2M1D05901780405250
MQA2DSLAX4M1D05901780405335
MQA2DSLAX4L1D05901780405342
59017804MQA2DSL705901780405359
MQA2DSLAX5M1D05901780405373
MQA2DSLAX3S1D05901780405281
MQA2DSLAX2L1D05901780405267
MQA2DSLAX3XLD05901780405311
MQA2DSLAX2XLD05901780405274
MQA2DSLAX3M1D05901780405298
MQA2DSLAX3L1D05901780405304
MQA2DSLAX2S1D05901780405243
MQA2DSLAX5L1D05901780405380