# Otovent® 50105

> Active: United States. Medical device record on deviCERTS, compiled from public registries.

- Canonical page: <https://devicerts.com/devices/otovent-r-50105>
- Manufacturer: [Circius Pharma AB](https://devicerts.com/manufacturers/circius-pharma-ab) (Sweden)
- Device class: Unclassified (US FDA)
- FDA product code: MJV
- GMDN: Middle ear decompressor, positive pressure (47542)

## Registrations and authorizations

- **GUDID** · GUDID listing · United States · UDI-DI 07350133960232 · listed 2026-08-20 · status: Listed (GUDID: in commercial distribution)
- **GUDID** · FDA 510(k) · United States · K920840 · decision 1992-10-05 · decision SESE · status: Active · from GUDID

## Recalls

No recall on record.

## Identity

- Trade name: Otovent® [FDA GUDID (AccessGUDID)]
- Generic name: Middle ear decompressor, positive pressure [FDA GUDID (AccessGUDID)]
- Model / reference: 50105 [FDA GUDID (AccessGUDID)]
- Description: Treatment of negative pressure in the middle ear. Otovent® can be used by adults and in children aged 3 years and up. 1 nose piece 1 balloon [FDA GUDID (AccessGUDID)]

## Identifiers

- Primary DI / UDI-DI: 07350133960232 [FDA GUDID (AccessGUDID)]
- 510(k) Number: K920840 [FDA GUDID (AccessGUDID)]
- FDA product code: MJV [FDA GUDID (AccessGUDID)]
- GMDN term: Middle ear decompressor, positive pressure (47542) [FDA GUDID (AccessGUDID)]

## Classification

- Device class: U [FDA GUDID (AccessGUDID)]
- GUDID distribution status: In Commercial Distribution [FDA GUDID (AccessGUDID)]

## Properties

- Contains latex: Yes [FDA GUDID (AccessGUDID)]
- Prescription use: Yes [FDA GUDID (AccessGUDID)]
- Over-the-counter: Yes [FDA GUDID (AccessGUDID)]
- Lot / batch number: Yes [FDA GUDID (AccessGUDID)]
- Expiration date: Yes [FDA GUDID (AccessGUDID)]
- Manufacturing date: Yes [FDA GUDID (AccessGUDID)]
- Supplied sterile: No [FDA GUDID (AccessGUDID)]
- Sterilise before use: No [FDA GUDID (AccessGUDID)]
- Single use: No [FDA GUDID (AccessGUDID)]
- Implantable: No [FDA GUDID (AccessGUDID)]
- Convenience kit: No [FDA GUDID (AccessGUDID)]
- Combination product: No [FDA GUDID (AccessGUDID)]
- HCT/P: No [FDA GUDID (AccessGUDID)]
- Premarket exempt: No [FDA GUDID (AccessGUDID)]
- Serial number: No [FDA GUDID (AccessGUDID)]

## Source and citation

- Cite as: Otovent® 50105, Circius Pharma AB. deviCERTS medical device catalogue. https://devicerts.com/devices/otovent-r-50105 (data as of 2026-11-15).
- Data sources: [FDA GUDID (AccessGUDID)](https://accessgudid.nlm.nih.gov/)
- Registry records last synced: 2026-10-23
- Statuses computed as of: 2026-11-15
- JSON: <https://devicerts.com/devices/otovent-r-50105.json>
- Licence: [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/). The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.
- Attribution: DevicErts, https://devicerts.com/devices/otovent-r-50105
- Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails.