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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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AROMAFORCE EXTRA COUGH SYRUP — 5 UDI-DI variants, MDR

MD Atlas
PRANARÔM ESPAÑA S.L.U

Data from EUDAMED, last updated May 23, 2026

AROMAFORCE EXTRA COUGH SYRUP

8437023771SYRUPG46P

5 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: PRANARÔM ESPAÑA S.L.U

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8437023771SYRUPG46P
Device name: AROMAFORCE EXTRA COUGH SYRUP
Device model: SYRUPG4
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 6, 2026

Manufacturer & authorised representative

Manufacturer

Name: PRANARÔM ESPAÑA S.L.U
SRN: ES-MF-000014215
Country: Spain
Email: gpujol@pranarom.com
Phone: +34 670 68 21 41

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01K598FZQHTQX5M80FEY9PBNVM

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

2327208437023771488
2286208437023771266
2327008437023771471
2287008437023771273
2338108437023771495