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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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Scar gel/Żel na blizny — 4 UDI-DI variants, MDR

MD Atlas
Gofarm Sp. z o.o. Sp. k.

Data from EUDAMED, last updated May 30, 2026

Scar gel/Żel na blizny

5906395089SC079W

4 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: Gofarm Sp. z o.o. Sp. k.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5906395089SC079W
Device name: Scar gel/Żel na blizny
Device model: 20g,15g
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 11, 2024

Manufacturer & authorised representative

Manufacturer

Name: Gofarm Sp. z o.o. Sp. k.
SRN: PL-MF-000003485
Country: Poland
Email: office@gofarm.pl
Phone: +48 530 103 518

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01H8NXQNHF9AAVHTB011B2X8Z2

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

SC0704260600590240
Nascar gel05060461191018
SC0705903769501403
SC0705903769500857