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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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Pokrowiec medyczny — 10 UDI-DI variants, MDR

MD Atlas
JAMTEX SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ

Data from EUDAMED, last updated May 30, 2026

Pokrowiec medyczny

5905538123pokrowiecSH

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: JAMTEX SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5905538123pokrowiecSH
Device name: Pokrowiec medyczny
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: JAMTEX SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ
SRN: PL-MF-000052121
Country: Poland
Email: biuro@jamtex.pl
Phone: +48 602 765 584

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01KJ2S42X4GS7YEJJV7AW5B22D

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

160x20005904720171369
140x20005904720171079
90x200x1205905538123670
90x200x805905538123663
90x200x1505905538123687
90x200x1005905538123656
90x200x1705905538123694
50x7005904720171024
70x8005904720171055
50x6005904720171031