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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 — 7 UDI-DI variants, MDR (HERBOLIVA 10 S.L.)

MD Atlas
HERBOLIVA 10 S.L.

Data from EUDAMED, last updated May 23, 2026

FARMOLIVA OLEICOPIEL

8437015720OLEICOPIELDZ

7 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: 8437015720OLEICOPIELDZ
Device name: FARMOLIVA OLEICOPIEL
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 4, 2025

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

7 UDI-DI variants

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Applied filters

basicUdiUlid01HF7FZRQKQFBXKS2B76KEDY0B

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

163601008437015720012
173115908437015720005
173116008437015720081
173116108437015720098
192969308437015720029
193110108437015720104
163602018437015720514