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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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KICK THE TICK® expert ZESTAW DO… — 6 UDI-DI variants, MDR

MD Atlas
ICB Pharma spółka z ograniczoną odpowiedzialnością

Data from EUDAMED, last updated May 31, 2026

KICK THE TICK® expert ZESTAW DO BEZPIECZNEGO USUWANIA KLESZCZY

590421527KTTExpertP2

6 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: ICB Pharma spółka z ograniczoną odpowiedzialnością

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 590421527KTTExpertP2
Device name: KICK THE TICK® expert ZESTAW DO BEZPIECZNEGO USUWANIA KLESZCZY
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 27, 2025

Manufacturer & authorised representative

Manufacturer

Name: ICB Pharma spółka z ograniczoną odpowiedzialnością
SRN: PL-MF-000007145
Country: Poland
Email: barbara.kubin@icbpharma.com

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K8JFR7YVX9JRM6QC3RFAYMNW

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

655504260762340240
KICK THE TICK® expert05904215274094
776005904215273561
864205904993491423
None05904215272953
681905703071020780