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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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GUANTE DE NITRILO SIN POLVO NO ESTÉRIL — 7 UDI-DI variants, MDR

MD Atlas
CELULOSAS VASCAS, S. L.

Data from EUDAMED, last updated May 23, 2026

GUANTE DE NITRILO SIN POLVO NO ESTÉRIL

8435027GNNFD

7 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: CELULOSAS VASCAS, S. L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8435027GNNFD
Device name: GUANTE DE NITRILO SIN POLVO NO ESTÉRIL
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 12, 2026

Manufacturer & authorised representative

Manufacturer

Name: CELULOSAS VASCAS, S. L.
SRN: ES-MF-000014657
Country: Spain
Email: calidad@cvprotection.com

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01HBATJZ9YG1C6AK56H4HN9JQ4

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

GNN.00X.1018435027100997
GNN.0XP.1018435027123309
GNN.BLACKX.1018435027123262
GNN.T0X.1118435027123255
10012401_X18435027123279
GNN.APX.5018435027123217
GST-N0000X18435027123231