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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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Blizcare gel — 2 UDI-DI variants, MDR

MD Atlas
Topsil Med Spółka z Ograniczoną Odpowiedzialnością

Data from EUDAMED, last updated May 30, 2026

Blizcare gel

5906874445gelQW

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: Topsil Med Spółka z Ograniczoną Odpowiedzialnością

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5906874445gelQW
Device name: Blizcare gel
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 2, 2023

Manufacturer & authorised representative

Manufacturer

Name: Topsil Med Spółka z Ograniczoną Odpowiedzialnością
SRN: PL-MF-000036040
Country: Poland
Email: kontakt@topsilmed.com
Phone: + 48 46 819 30 71

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HDGG6XQ438D538Y3M10678RS

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

8SP-007505906874445310
8SP-002805906874445006