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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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Otovent — 13 UDI-DI variants, MDR (Circius Pharma AB)

MD Atlas
Circius Pharma AB

Data from EUDAMED, last updated May 30, 2026

Otovent

735013396Otovent1TV

13 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: Circius Pharma AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 735013396Otovent1TV
Device name: Otovent
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 21, 2025

Manufacturer & authorised representative

Manufacturer

Name: Circius Pharma AB
SRN: SE-MF-000013023
Country: Sweden
Email: info@circiuspharma.com
Phone: +46 31 818400

Variants by status

UDI-DI variants

13 UDI-DI variants

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Applied filters

basicUdiUlid01KAJY8BWZFADEYC8FTJ0Q1NW0

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

5050207350133960096
5010107350133960218
5150107350133960195
5050307350133960089
5050807350133960607
5010607350133960584
5050407350133960119
5550507350133960904
5010207350133960201
5050107350133960102
5050707350133960140
5010307350133960249
5011007350133960942