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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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syntic — 3 UDI-DI variants, MDR (tic Medizintechnik GmbH)

MD Atlas
tic Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

syntic

426021766-T-PLSH

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: tic Medizintechnik GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426021766-T-PLSH
Device name: syntic
Device model: PremiumLINE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: tic Medizintechnik GmbH
SRN: DE-MF-000033923
Country: Germany
Email: info@ticmed.de
Phone: +49236920850

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KGKWHDKAH6J4TCKQYBSZF1B2

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

ti200804260217666208
ti100404260217666185
ti100304260217666192