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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 SYRUP ADULT — 10 UDI-DI variants, MDR

MD Atlas
STE PHARMACEUTICALS, S.L.U

Data from EUDAMED, last updated May 23, 2026

COUGH SYRUP ADULT

843654262PL01458Z

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: STE PHARMACEUTICALS, S.L.U

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 843654262PL01458Z
Device name: COUGH SYRUP ADULT
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: STE PHARMACEUTICALS, S.L.U
SRN: ES-MF-000000144
Country: Spain
Email: ihernandez@stepharmaceuticals.com
Phone: +34 935923100

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01KQ9Q93GHYR7KDE4337MMN0NH

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

PL0145_14008436542627474
PL0145_14008595566424305
PL0145_14005202888331008
PL0145_14008435232358926
PL0145_14008436542626026
PL0145_STICK08436617646553
PL0145_12008436617643163
PL0145_14008436542626019
PL0145_STICK08436617646539
PL0145_12008436617643149