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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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Leica DB80 HS, LS, LX; 818, 819 — 5 UDI-DI variants, IVDR

MD Atlas
Leica Biosystems Nussloch GmbH

Data from EUDAMED, last updated May 23, 2026

Leica DB80 HS, LS, LX; 818, 819

010404918803589W

5 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: Leica Biosystems Nussloch GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 010404918803589W
Device name: Leica DB80 HS, LS, LX; 818, 819
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Apr 19, 2022

Manufacturer & authorised representative

Manufacturer

Name: Leica Biosystems Nussloch GmbH
SRN: DE-MF-000021943
Country: Germany
Email: support.de@LeicaBiosystems.com
Phone: +49 6224 143 0

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01G10G9ZZ9D777JTNZBVEY72BA

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

1403583892604049188114587
1403583892504049188114594
1403584349004049188159496
1403584348804049188159465
1403584349604049188159526