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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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Surgical light system — 5 UDI-DI variants, MDR (Merivaara Corporation)

MD Atlas
Merivaara Corporation

Data from EUDAMED, last updated May 23, 2026

Surgical light system

643843521RC

5 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: Merivaara Corporation

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 643843521RC
Device name: Surgical light system
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 17, 2022

Manufacturer & authorised representative

Manufacturer

Name: Merivaara Corporation
SRN: FI-MF-000001175
Country: Finland
Email: merivaara@merivaara.com
Phone: +358 3 3394611

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01G2YQTF3Z6H30XA4TAJ2VCAY6

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

52022206438435202227
52021106438435202111
520400006438435040003
52021006438435202104
52023006438435202302