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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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REUSABLE INCONTINENCE PRODUCTS — 8 UDI-DI variants, MDR

MD Atlas
TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA

Data from EUDAMED, last updated May 31, 2026

REUSABLE INCONTINENCE PRODUCTS

5900516AAZZXXX23

8 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: TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5900516AAZZXXX23
Device name: REUSABLE INCONTINENCE PRODUCTS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA
SRN: PL-MF-000002200
Country: Poland
Email: biuro.zarzadu@tzmo-global.com
Phone: +48 56 612 39 00

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01KM0G7N8BW7V134YNTFQ3PVWG

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

SE-W96-M001-LB105900516747015
SE-W96-S001-LB105900516746995
SE-W96-L001-LB105900516747039
SE-W96-XL01-LB105900516747053
SE-W96-2X01-MB105900516755072
SE-W96-L001-MB105900516755010
SE-W96-M001-MB105900516754990
SE-W96-XL01-MB105900516755034