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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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Materac Szpitalny — 5 UDI-DI variants, MDR

MD Atlas
JAMTEX SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ

Data from EUDAMED, last updated May 30, 2026

Materac Szpitalny

5904720171materac3J

5 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: 5904720171materac3J
Device name: Materac Szpitalny
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

5 UDI-DI variants

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Applied filters

basicUdiUlid01KJ2QHQEFZR1XVZGXRGK9KT59

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

90x200x1005905538123991
90x200x1205904720171284
90x200x1505904720171000
90x200x1705904720171178
90x200x805904720171017