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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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Quark RMR — 1 UDI-DI variant, MDR (COSMED Srl)

MD Atlas
COSMED Srl

Data from EUDAMED, last updated May 30, 2026

Quark RMR

805240018QRMRAV

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: COSMED Srl

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 805240018QRMRAV
Device name: Quark RMR
Device model: Quark series
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 6, 2024

Manufacturer & authorised representative

Manufacturer

Name: COSMED Srl
SRN: IT-MF-000023488
Country: Italy
Email: regulatory@cosmed.com

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01JC0GCXS658CE2M3GQ5ETT57G

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

C09074-01-9918052400180171