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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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TUBO GEL RIZO — 9 UDI-DI variants, MDR (LABORATORIOS HERBITAS, S.L.)

MD Atlas
LABORATORIOS HERBITAS, S.L.

Data from EUDAMED, last updated May 23, 2026

TUBO GEL RIZO

84351355RIZOUE

9 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: 84351355RIZOUE
Device name: TUBO GEL RIZO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 16, 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

9 UDI-DI variants

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Applied filters

basicUdiUlid01JAAR9KE81EP1CT71KTQKG675

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

11.053.1408435135523025
11.053.1208435135506509
11.053.208435135577257
11.053.108435135577240
6011.608435135507292
6011.508435135506479
6011.708435135523018
11.053.308435135577264
11.053.1108435135506493