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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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Formówki sekcyjne tytanowe — 6 UDI-DI variants, MDR

MD Atlas
VESTON DARIUSZ KAWALEC

Data from EUDAMED, last updated May 30, 2026

Formówki sekcyjne tytanowe

59059731076sektytanU4

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: VESTON DARIUSZ KAWALEC

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 59059731076sektytanU4
Device name: Formówki sekcyjne tytanowe
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 14, 2023

Manufacturer & authorised representative

Manufacturer

Name: VESTON DARIUSZ KAWALEC
SRN: PL-MF-000038627
Country: Poland
Email: biuroveston@o2.pl
Phone: +48 888 019 137

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HHKT14WQV16J4NNHCKFBEGMH

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

T-01 - małe05906124397161
T-02 - średnie05906124397178
T-0205906124397499
T-0305906124397505
T-0105906124397482
T-03 - duże05906124397185