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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 LUMBOSACRA EXTRA — 4 UDI-DI variants, MDR

MD Atlas
Laboratorios Cinfa, S.A.

Data from EUDAMED, last updated May 23, 2026

FARMALASTIC FAJA LUMBOSACRA EXTRA

8430469fajasacrolumbarAC

4 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: 8430469fajasacrolumbarAC
Device name: —
Device model: FARMALASTIC FAJA LUMBOSACRA EXTRA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 3, 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

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KGHAWV81GFR2MYDW7H8FPKSC

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

269142.108430469691181
269134.608430469691266
269126.108430469691341
269118.608430469691426