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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 nitrilo — 3 UDI-DI variants, MDR (Oasipor - Medical, S.A.)

MD Atlas
Oasipor - Medical, S.A.

Data from EUDAMED, last updated May 30, 2026

Luvas de nitrilo

560032008LN91XVX

3 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: Oasipor - Medical, S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 560032008LN91XVX
Device name: —
Device model: Luvas de nitrilo
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: Oasipor - Medical, S.A.
SRN: PT-MF-000002957
Country: Portugal
Email: geral@oasipor.pt
Phone: +351 252 499 070

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KQ7S8Y65Y8QM6D10QNZ1JBMS

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

Nitrile gloves, powder free - L05600320080024
Nitrile gloves, powder free - M05600320080017
Nitrile gloves, powder free - S05600320080000