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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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LYNXERA LS35, LN35, LA35, XA35, XN35,… — 6 UDI-DI variants, IVDR

MD Atlas
Lutz GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

LYNXERA LS35, LN35, LA35, XA35, XN35, XS35

4260758246067YZ

6 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: Lutz GmbH & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4260758246067YZ
Device name: LYNXERA LS35, LN35, LA35, XA35, XN35, XS35
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Dec 10, 2025

Manufacturer & authorised representative

Manufacturer

Name: Lutz GmbH & Co. KG
SRN: DE-MF-000038332
Country: Germany
Email: cornelia.bahrmann@lutz-blades.com

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01JC099SMB2J90ZFKFMACBD2PX

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

1007484804260758240431
1007484604260758240448
1007484704260758240455
1007472304260758240462
1007472104260758240479
1007472204260758240486