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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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ZARBEE’S SYRUP — 10 UDI-DI variants, MDR (Labomar S.p.A.)

MD Atlas
Labomar S.p.A.

Data from EUDAMED, last updated May 30, 2026

ZARBEE’S SYRUP

805630062FTPR101DK

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: 805630062FTPR101DK
Device name: ZARBEE’S SYRUP
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jul 26, 2023

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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Export results

Applied filters

basicUdiUlid01H68HTWV0PV2DN46X8Z7QD75V

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

FTPR10108056300620655
FTPR10108056300621157
FTPR10108056300621140
FTPR10108056300621294
Benylin 150 ml UK, IRL08056300621904
Benylin 250 ml UK, IRL08056300621911
FTPR10108056300620648
FTPR10108056300621287
FTPR10108056300620662
Zarbeil Syrup 150 ml FR08056300620631