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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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non-sterile cohesive bandage — 2 UDI-DI variants, MDR

MD Atlas
ZARYS International Spółka z ograniczoną odpowiedzialnością

Data from EUDAMED, last updated May 31, 2026

non-sterile cohesive bandage

59079968M03040202HL

2 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: ZARYS International Spółka z ograniczoną odpowiedzialnością

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 59079968M03040202HL
Device name: non-sterile cohesive bandage
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 30, 2026

Manufacturer & authorised representative

Manufacturer

Name: ZARYS International Spółka z ograniczoną odpowiedzialnością
SRN: PL-MF-000000410
Country: Poland
Email: zarys@zarys.pl
Phone: +48 32 376 07 20

Variants by status

UDI-DI variants

2 UDI-DI variants

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basicUdiUlid01KG7BWATR4D73SZPNBWNVSQEP

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

yellowBAND Cohesive bandage05907996880348
yellowBAND Cohesive bandage05907996880331