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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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Stethoscope — 6 UDI-DI variants, MDR (Rossmax Swiss GmbH)

MD Atlas
Rossmax Swiss GmbH

Data from EUDAMED, last updated May 31, 2026

Stethoscope

764020721StethoscopeUW

6 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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 764020721StethoscopeUW
Device name: Stethoscope
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 25, 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

6 UDI-DI variants

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Applied filters

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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

Stethoscope07640207210029
Stethoscope07640207210043
Stethoscope07640207210036
Stethoscope07640207210265
Stethoscope07640207210012
Stethoscope07640207210258