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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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Cough Treatment Spray — 2 UDI-DI variants, MDR

MD Atlas
Medical Brands Developments BV

Data from EUDAMED, last updated May 31, 2026

Cough Treatment Spray

872064894040HG

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Medical Brands Developments BV

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Device characteristics

Active device

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 872064894040HG
Device name: —
Device model: Cough Treatment Spray
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: Medical Brands Developments BV
SRN: NL-MF-000002672
Country: Netherlands
Email: qara@medicalbrands.com
Phone: +31 20 3455330

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KSN2H8TQWF9DF3A7YN4Z9SE5

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

BiSeptol Junior Spray 20ml, RO05940541562139
20TSEE.KF.HU04008617989615