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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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AIR-X — 18 UDI-DI variants, MDR (UNIVET LOUPES SPA)

MD Atlas
UNIVET LOUPES SPA

Data from EUDAMED, last updated May 31, 2026

AIR-X

8057147FUP001T4

18 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 LOUPES SPA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8057147FUP001T4
Device name: —
Device model: AIR-X
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 LOUPES SPA
SRN: IT-MF-000027104
Country: Italy
Email: martina.marzotto@univetloupes.com

Variants by status

UDI-DI variants

18 UDI-DI variants

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Applied filters

basicUdiUlid01KRZYBW1NHAF0C1BRBAN2DX2F

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

KK84035.0A08057147000051
KK85836.0A08057147000150
KK83635.0A08057147000013
KK85736.0A08057147000143
KK84535.0A08057147000105
KK84635.0A08057147000112
KK83735.0A08057147000020
KK84435.0A08057147000099
KK85636.0A08057147000136
KK85936.0A08057147000167
KK83935.0A08057147000044
KK84235.0A08057147000075
KK83535.0A08057147000006
KK84735.0A08057147000129
KK83835.0A08057147000037
KK84335.0A08057147000082
KK86036.0A08057147000174
KK84135.0A08057147000068