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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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NOSA smell training — 1 UDI-DI variant, MDR (NoseOption AB)

MD Atlas
NoseOption AB

Data from EUDAMED, last updated May 30, 2026

NOSA smell training

73500817804NX

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: NoseOption AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 73500817804NX
Device name: NOSA smell training
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 28, 2024

Manufacturer & authorised representative

Manufacturer

Name: NoseOption AB
SRN: SE-MF-000025669
Country: Sweden
Email: alexis.ruin@nosaplugs.com

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01J1F9KB2S39A9FCWG0PPH6XEW

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

40004160107350081780395