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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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Spacer for Aerosol — 4 UDI-DI variants, MDR (Rossmax Swiss GmbH)

MD Atlas
Rossmax Swiss GmbH

Data from EUDAMED, last updated May 30, 2026

Spacer for Aerosol

764020721AerospacerJ9

4 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: Rossmax Swiss GmbH

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 764020721AerospacerJ9
Device name: Spacer for Aerosol
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Rossmax Swiss GmbH
SRN: CH-MF-000011245
Country: Switzerland
Email: info@rossmax.com

Authorised representative

Name: CMC Medical Devices & Drugs SL
SRN: ES-AR-000000293
Country: Spain
Phone: +34951214054

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KSHKNK88HBSDC3GT29FM3101

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

Spacer for Aerosol07640207210081
Spacer for Aerosol07640207210050
Spacer for Aerosol07640207210074
Spacer for Aerosol07640207210067