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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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FARMOLIVA OLEICOPIEL HIPEROXIGENADO — 8 UDI-DI variants, MDR

MD Atlas
HERBOLIVA 10 S.L.

Data from EUDAMED, last updated May 23, 2026

FARMOLIVA OLEICOPIEL HIPEROXIGENADO

8437015720OLEICOHIPECU

8 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: HERBOLIVA 10 S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8437015720OLEICOHIPECU
Device name: FARMOLIVA OLEICOPIEL HIPEROXIGENADO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 20, 2023

Manufacturer & authorised representative

Manufacturer

Name: HERBOLIVA 10 S.L.
SRN: ES-MF-000038660
Country: Spain
Email: tecnico@herboliva10.com

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01HFC7GXW3DJPBEEWHM1D26BAY

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

202306018437015720521
202305608437015720159
202305108437015720166
202305208437015720111
202305308437015720128
202305408437015720135
202305508437015720142
202306118437015720538