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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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Microscope Software — 2 UDI-DI variants, IVDR

MD Atlas
Carl Zeiss Microscopy GmbH

Data from EUDAMED, last updated May 23, 2026

Microscope Software

4064897DEA006JX

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: Carl Zeiss Microscopy GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4064897DEA006JX
Device name: Microscope Software
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Special device type: refdata.special-ivd-device-type.software
Version date: Jul 11, 2022

Manufacturer & authorised representative

Manufacturer

Name: Carl Zeiss Microscopy GmbH
SRN: DE-MF-000024424
Country: Germany
Email: regulatoryaffairs.microscopy@zeiss.com
Phone: +49 3641 64 0

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01G7PTVM6XZBASJNXK9CP66MP3

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

410135-0052-46004064897000372
Labscope 4.704064897000396