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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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Luvas de exame — 19 UDI-DI variants, MDR (Hasse, SA)

MD Atlas
Hasse, SA

Data from EUDAMED, last updated May 31, 2026

Luvas de exame

5604427GLOVESWE

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: Hasse, SA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5604427GLOVESWE
Device name: Luvas de exame
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 6, 2026

Manufacturer & authorised representative

Manufacturer

Name: Hasse, SA
SRN: PT-MF-000005662
Country: Portugal
Email: comercial@hasse.pt
Phone: +351 26 351 94 49

Variants by status

UDI-DI variants

19 UDI-DI variants

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Applied filters

basicUdiUlid01KQYVEM6F1Y56E9F1JRBMBJNF

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

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745705604427079066
745805604427079073
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745605604427075563
744805604427079653
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745005604427079677
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744105604427079097
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