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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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MD COUGH SYRUP sugar free — 10 UDI-DI variants, MDR (Labomar S.p.A.)

MD Atlas
Labomar S.p.A.

Data from EUDAMED, last updated May 30, 2026

MD COUGH SYRUP sugar free

805630062FTPR659U

10 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: 805630062FTPR659U
Device name: MD COUGH SYRUP sugar free
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 11, 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

10 UDI-DI variants

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Applied filters

basicUdiUlid01JP283Y2XT92FBS8JCSY84BHR

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

FTPR6508056300620822
FTPR6508056300620846
Bisolnatural 3 in1 sans sucre /Zonder suiker / ohne Zucker 100 ml BE08056300620808
FTPR6508056300620815
FTPR6508056300621836
FTPR6508056300621799
FTPR6508056300621577
FTPR6508056300621898
Phytoxil toux sans sucre 100 ml FR08056300620792
FTPR6508056300621812