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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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FARMALASTIC MUÑEQUERA PULGAR… — 2 UDI-DI variants, MDR

MD Atlas
Laboratorios Cinfa, S.A.

Data from EUDAMED, last updated May 23, 2026

FARMALASTIC MUÑEQUERA PULGAR COMPRESSION TECH

8430469muneqmetapulgarXN

2 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: Laboratorios Cinfa, S.A.

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 8430469muneqmetapulgarXN
Device name: —
Device model: FARMALASTIC MUÑEQUERA PULGAR COMPRESSION TECH
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: Laboratorios Cinfa, S.A.
SRN: ES-MF-000001574
Country: Spain
Email: cinfa@cinfa.com
Phone: +34 948 33 50 05

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KG4HMRBH87VENDJFP41BECSM

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

159272.908430469203759
159273.608430469203766