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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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Coala Monitor — 1 UDI-DI variant, MDR (Coala Solutions AB)

MD Atlas
Coala Solutions AB

Data from EUDAMED, last updated May 31, 2026

Coala Monitor

735000270CoalaSystem001XV

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Coala Solutions AB

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 735000270CoalaSystem001XV
Device name: Coala Monitor
Device model: Coala Monitor Device M2
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Oct 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: Coala Solutions AB
SRN: SE-MF-000046932
Country: Sweden
Email: info@coalasolutions.com
Phone: +46852516011

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01K7S061D9P90EW4S2V53F5RXT

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

Coala Monitor73500027000992