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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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MUÑEQUERA METAPULGAR TALLA P-M-G — 3 UDI-DI variants, MDR

MD Atlas
VENTUBEL, S.A.

Data from EUDAMED, last updated May 31, 2026

MUÑEQUERA METAPULGAR TALLA P-M-G

8430487METAPULGARFK

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: VENTUBEL, S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8430487METAPULGARFK
Device name: MUÑEQUERA METAPULGAR TALLA P-M-G
Device model: MUÑEQUERA METAPULGAR TALLA P-M-G
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: VENTUBEL, S.A.
SRN: ES-MF-000039014
Country: Spain
Email: sduran@ventubel.com
Phone: +34916124401

Variants by status

UDI-DI variants

3 UDI-DI variants

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basicUdiUlid01KSHXTNP9TF94NR464T36T94H

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

MP G08430487000033
MP M08430487000026
MP P08430487000019