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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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536.08 — 19 UDI-DI variants, MDR (UNIVET SRL)

MD Atlas
UNIVET SRL

Data from EUDAMED, last updated May 31, 2026

536.08

8057147COR013QG

19 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: 8057147COR013QG
Device name: —
Device model: 536.08
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

19 UDI-DI variants

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Applied filters

basicUdiUlid01KS0EXEMXQG9C1Y897SJS0WMH

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

53608C096-PKI08057147045083
53608P09808057147045212
53608P09108057147045151
53608P098-PKI.08057147045243
53608C09808057147045120
53608C09308057147045069
53608P097-PKI08057147045205
53608C09608057147045076
53608C097.08057147045106
53608P09608057147045175
53608P098.08057147045229
53608C097-PKI08057147045113
53608C098.08057147045137
53608P09008057147045144
53608P096-PKI08057147045182
53608P09708057147045199
53608P098-PKI08057147045236
53608P09308057147045168
53608C09708057147045090