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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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OHA (Orthèse Herbst Amoric) — 14 UDI-DI variants, MDR (Fulcrum)

MD Atlas
Fulcrum

Data from EUDAMED, last updated May 19, 2026

OHA (Orthèse Herbst Amoric)

3770024630008UZ

14 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: Fulcrum

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3770024630008UZ
Device name: OHA (Orthèse Herbst Amoric)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 6, 2026

Manufacturer & authorised representative

Manufacturer

Name: Fulcrum
SRN: FR-MF-000015624
Country: France
Email: contact@fulcrum.fr
Phone: +33 (0)677067508

Variants by status

UDI-DI variants

14 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KGSS964SFHHF51HYPBB34RE5

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

OHA Orthèse Herbst Amoric C03770024630008
OHA Orthèse Herbst Amoric S03770024630176
1.303770024630152
2.103770024630077
1.403770024630145
1.7103770024630114
3.903770024630015
1.203770024630169
2.203770024630060
1.8203770024630084
1.7203770024630107
1.603770024630121
1.8103770024630091
1.503770024630138