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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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ORTESIS POSTQUIRURGICA — 6 UDI-DI variants, MDR

MD Atlas
LABORATORIOS HERBITAS, S.L.

Data from EUDAMED, last updated May 23, 2026

ORTESIS POSTQUIRURGICA

84360266POSTQUIRUR43

6 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: 84360266POSTQUIRUR43
Device name: ORTESIS POSTQUIRURGICA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 7, 2025

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

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K227EJNE9QP9RVGD7W2ZBNYQ

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

12.720.2308436026682524
12.720.2208436026682517
12.720.2408436026682531
12.720.2108436026682500
12.720.2508436026682548
12.720.2008436026682494