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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 ORTHO WEDGE — 5 UDI-DI variants, MDR

MD Atlas
LABORATORIOS HERBITAS, S.L.

Data from EUDAMED, last updated May 23, 2026

ORTESIS ORTHO WEDGE

84360266ORTHOWEDGES5

5 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: 84360266ORTHOWEDGES5
Device name: ORTESIS ORTHO WEDGE
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

5 UDI-DI variants

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Applied filters

basicUdiUlid01K21ZCR64F40YYA805H57A2M5

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

12.719.2108436026682562
12.719.2208436026682579
12.719.2408436026682593
12.719.2008436026682555
12.719.2308436026682586