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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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SEPARADOR 1/2 LUNA gel — 3 UDI-DI variants, MDR

MD Atlas
LABORATORIOS HERBITAS, S.L.

Data from EUDAMED, last updated May 23, 2026

SEPARADOR 1/2 LUNA gel

84351355LUNAGELWA

3 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: LABORATORIOS HERBITAS, S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84351355LUNAGELWA
Device name: SEPARADOR 1/2 LUNA gel
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 6, 2024

Manufacturer & authorised representative

Manufacturer

Name: LABORATORIOS HERBITAS, S.L.
SRN: ES-MF-000004599
Country: Spain
Email: herbitas@herbitas.com
Phone: +34 96 362 79 00

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01JC0BF3X8MVVJ89M4EEM7NWRW

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

6002.608435135500118
6002.708435135500125
6002.508435135500101