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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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PUREsthetic Matrix Bands — 4 UDI-DI variants, MDR

MD Atlas
VESTON DARIUSZ KAWALEC

Data from EUDAMED, last updated May 30, 2026

PUREsthetic Matrix Bands

59059731076PUREMatrixbdJK

4 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: 59059731076PUREMatrixbdJK
Device name: PUREsthetic Matrix Bands
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 22, 2024

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

4 UDI-DI variants

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Applied filters

basicUdiUlid01HSK7HX0PW3536H9WZDMXZ5VJ

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

PUREsthetic Matrix Bands Type 12 – premolars05906124397376
PUREsthetic Matrix Bands Type 13 – molars05906124397383
PUREsthetic Matrix Bands Type 8 – premolars05906124397352
PUREsthetic Matrix Bands Type 9 – molars05906124397369