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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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PROPOLIS NASAL SPRAY — 9 UDI-DI variants, MDR

MD Atlas
STE PHARMACEUTICALS, S.L.U

Data from EUDAMED, last updated May 23, 2026

PROPOLIS NASAL SPRAY

843654262PL008598

9 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: 843654262PL008598
Device name: PROPOLIS NASAL SPRAY
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

9 UDI-DI variants

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Applied filters

basicUdiUlid01KQ9Q8ECE51NEYC8KD3A0GJ64

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

PL008508436542624282
PL008508436617648366
PL008508436542626965
PL008503486330128749
PL008508436542626958
PL008508436542626996
PL008508426420909051
PL008508436617645532
PL008508436542626866