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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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FAJA LUMBAR ANCHA — 4 UDI-DI variants, MDR (Dyno Rechi)

MD Atlas
Dyno Rechi

Data from EUDAMED, last updated May 23, 2026

FAJA LUMBAR ANCHA

843582590114001S06NE

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: Dyno Rechi

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 843582590114001S06NE
Device name: FAJA LUMBAR ANCHA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: Dyno Rechi
SRN: ES-MF-000035525
Country: Spain
Email: dynorechi@dynorechi.com
Phone: +32 964223951

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KFJS33X29HEFRG1EWQE4WRVQ

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

0114003L0608435825900464
0114002M0608435825900457
0114001S0608435825900440
011404XL0608435825900471