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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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Labinlight Cartdrige — 2 UDI-DI variants, IVDR (LABINLIGHT, LDA)

MD Atlas
LABINLIGHT, LDA

Data from EUDAMED, last updated May 30, 2026

Labinlight Cartdrige

5600717621CARTDRIGE94

2 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: LABINLIGHT, LDA

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 5600717621CARTDRIGE94
Device name: Labinlight Cartdrige
Device model: H1000
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jun 25, 2024

Manufacturer & authorised representative

Manufacturer

Name: LABINLIGHT, LDA
SRN: PT-MF-000034199
Country: Portugal
Email: info@labinlight.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J17JDGMZ6YJXPPQTMVNWE03R

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

H10010005600717621045
H10005005600717621038