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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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PROVEO 8 — 3 UDI-DI variants, MDR (Leica Microsystems (Schweiz) AG)

MD Atlas
Leica Microsystems (Schweiz) AG

Data from EUDAMED, last updated May 23, 2026

PROVEO 8

76300035PROVEO8RV

3 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: 76300035PROVEO8RV
Device name: PROVEO 8
Device model: PROVEO 8
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

3 UDI-DI variants

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Applied filters

basicUdiUlid01K9RD99EYK3T9E0T4KQ84D7E8

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

PROVEO 8 - Ceiling Mount07630003587937
PROVEO 8 - OCT Ready07630003599008
PROVEO 8 - Optics Carrier07630003581799