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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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EUCALIPTOL — 2 UDI-DI variants, MDR (J RIPOLL SL)

MD Atlas
J RIPOLL SL

Data from EUDAMED, last updated May 23, 2026

EUCALIPTOL

843604224EUCALIPTOL32

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: J RIPOLL SL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 843604224EUCALIPTOL32
Device name: EUCALIPTOL
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: J RIPOLL SL
SRN: ES-MF-000001256
Country: Spain
Email: info@dentaflux.com
Phone: +34916289399

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KQ9XD00S53C86E5CY3WHM8GB

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

Eucalyptol 20 ml, Clinix08436042242603
Eucalyptol 20 ml, Dentaflux08436042240470