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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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Q-NRG — 8 UDI-DI variants, MDR (COSMED Srl)

MD Atlas
COSMED Srl

Data from EUDAMED, last updated May 30, 2026

Q-NRG

805240018QNRGA2

8 UDI-DI variants

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: 805240018QNRGA2
Device name: Q-NRG
Device model: Q-NRG series
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 4, 2024

Manufacturer & authorised representative

Manufacturer

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

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JBVQE9YB9KWRJYFJBGTXY737

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

C09092-21-9918052400181192
C09092-01-9918052400180508
C09092-11-9918052400180522
C09092-42-9918052400181307
C09092-12-9918052400180539
C09092-32-9918052400181291
C09092-22-9918052400181208
C09092-02-9918052400180515