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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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M822 — 4 UDI-DI variants, MDR (Leica Microsystems (Schweiz) AG)

MD Atlas
Leica Microsystems (Schweiz) AG

Data from EUDAMED, last updated May 23, 2026

M822

76300035M822DL

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: Leica Microsystems (Schweiz) AG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 76300035M822DL
Device name: M822
Device model: M822
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 11, 2025

Manufacturer & authorised representative

Manufacturer

Name: Leica Microsystems (Schweiz) AG
SRN: CH-MF-000021185
Country: Switzerland
Email: georges.hakim@leica-microsystems.com

Authorised representative

Name: Leica Microsystems CMS GmbH
SRN: DE-AR-000021052
Country: Germany

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01K9RF93RNSV6W1FKSZNPQMA0Z

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

M822 - Optics Carrier07630003568707
M822 CT4007630003526295
M822 F2007630003568752
M822 F4007630003526233