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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 — 31 UDI-DI variants, MDR

MD Atlas
P.P.H.U Prosport S.C Joanna i Antoni Dobija

Data from EUDAMED, last updated May 31, 2026

Materac Szpitalny

59038298szpitalny72

31 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: P.P.H.U Prosport S.C Joanna i Antoni Dobija

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 59038298szpitalny72
Device name: Materac Szpitalny
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: P.P.H.U Prosport S.C Joanna i Antoni Dobija
SRN: PL-MF-000043798
Country: Poland
Email: biuro@materace-sportowe.pl
Phone: +48691476515

Variants by status

UDI-DI variants

31 UDI-DI variants

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Applied filters

basicUdiUlid01KK3XF6F1KD433R5FM9WTJAXY

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

T25 200x90x10 cm 05903829802457
T35 200x80x12 cm 05903829802624
T35 200x90x12 cm 05903829802631
T35 195x90x15 cm05903829802594
T35 195x80x12 cm 05903829802655
T30 195x90x12 cm 05903829802556

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