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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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Children Cough syrup — 4 UDI-DI variants, MDR (Labomar S.p.A.)

MD Atlas
Labomar S.p.A.

Data from EUDAMED, last updated May 30, 2026

Children Cough syrup

805630062FTPR389R

4 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: Labomar S.p.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805630062FTPR389R
Device name: Children Cough syrup
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 12, 2025

Manufacturer & authorised representative

Manufacturer

Name: Labomar S.p.A.
SRN: IT-MF-000007965
Country: Italy
Email: regulatoryMD@labomar.com
Phone: +3904227312

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01K9VR9NQR3JMTETP5MGQN1NSG

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

FTPR3808056300621003
FTPR3808056300621041
FTPR3808056300621058
FTPR3808056300621553