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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 FAJA ABDOMINAL 3 BANDAS — 3 UDI-DI variants, MDR

MD Atlas
Laboratorios Cinfa, S.A.

Data from EUDAMED, last updated May 23, 2026

FARMALASTIC FAJA ABDOMINAL 3 BANDAS

8430469fajaabdom3bandasAL

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: Laboratorios Cinfa, S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8430469fajaabdom3bandasAL
Device name: FARMALASTIC FAJA ABDOMINAL 3 BANDAS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 18, 2022

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

3 UDI-DI variants

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Applied filters

basicUdiUlid01G3B6STYT1H3YB7PW642WZ51M

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

207494.108430469228158
207493.408430469228141
207492.708430469228134