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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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Operating Table / Non-active — 3 UDI-DI variants, MDR

MD Atlas
Merivaara Corporation

Data from EUDAMED, last updated May 23, 2026

Operating Table / Non-active

64384350535RZ

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: Merivaara Corporation

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 64384350535RZ
Device name: Operating Table / Non-active
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 23, 2021

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

3 UDI-DI variants

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Applied filters

basicUdiUlid01FJV1WAD6Q25YK5H4TPF96CDE

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

10003001006438435300107
10000186506438435018651
10000186006438435018606