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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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539 — 36 UDI-DI variants, MDR (UNIVET SRL)

MD Atlas
UNIVET SRL

Data from EUDAMED, last updated May 31, 2026

539

8057147COR014QJ

36 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: UNIVET SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8057147COR014QJ
Device name: —
Device model: 539
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 19, 2026

Manufacturer & authorised representative

Manufacturer

Name: UNIVET SRL
SRN: IT-MF-000030077
Country: Italy
Email: info@univet.it

Variants by status

UDI-DI variants

36 UDI-DI variants

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Applied filters

basicUdiUlid01KS0F1MQAQ743BT8RC3EMQNX1

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

539P00198-A+A08057147045502
539P00198-PKI08057147045526
539C00197.08057147045281
539P0019608057147045410
539P0139808057147045595
539C0019708057147045274
539P00198-A+A.08057147045519
539C0139608057147045335
539P00197.08057147045458
539P00198.08057147045496
539P00197-A+A08057147045465

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