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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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TTM Rozsdamentes infúziós pumpa… — 2 UDI-DI variants, MDR

MD Atlas
TakTiMed Egészségügyi, Kereskedelmi és Szolgáltató Kft.

Data from EUDAMED, last updated May 24, 2026

TTM Rozsdamentes infúziós pumpa dokkoló tartó állványok

5999862367AllvanyokTM

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: TakTiMed Egészségügyi, Kereskedelmi és Szolgáltató Kft.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5999862367AllvanyokTM
Device name: TTM Rozsdamentes infúziós pumpa dokkoló tartó állványok
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 13, 2023

Manufacturer & authorised representative

Manufacturer

Name: TakTiMed Egészségügyi, Kereskedelmi és Szolgáltató Kft.
SRN: HU-MF-000029587
Country: Hungary
Email: info@taktimed.hu
Phone: +36 70 210 0022

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01H572D21EWMM3HZRZRJWPXKYC

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

TTM01105999862367008
TTM01205999862367015