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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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Oscilla® AudioConsole® — 1 UDI-DI variant, MDR (Oscilla A/S)

MD Atlas
Oscilla A/S

Data from EUDAMED, last updated May 31, 2026

Oscilla® AudioConsole®

5745000311SW01VH

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: Oscilla A/S

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Device characteristics

Measuring functionAdministers medicine

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 5745000311SW01VH
Device name: Oscilla® AudioConsole®
Device model: SW01
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 27, 2024

Manufacturer & authorised representative

Manufacturer

Name: Oscilla A/S
SRN: DK-MF-000002784
Country: Denmark
Email: info@oscilla.dk
Phone: +45 61728170

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01HN5W36A12HXMJWHHB57PZY3F

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

Oscilla® AudioConsole®05745000311033