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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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Plancha siligel — 10 UDI-DI variants, MDR

MD Atlas
LABORATORIOS HERBITAS, S.L.

Data from EUDAMED, last updated May 23, 2026

Plancha siligel

84351355SILIGELW7

10 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: 84351355SILIGELW7
Device name: Plancha siligel
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

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JAAG2KYRXKN4WRQ22FZ7FWYG

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

11.021.608435135517680
11.052.708436026686232
11.052.1108435135504246
11.052.1008435135504239
11.052.908435135504390
10.052.308435135504345
11.052.1208435135504253
11.052.408435135504352
11.052.508435135504369
11.052.608435135504376