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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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Ankle Stirrup-Junior Air — 73 UDI-DI variants, MDR (Orthobroker)

MD Atlas
Orthobroker

Data from EUDAMED, last updated May 23, 2026

Ankle Stirrup-Junior Air

5404020402anklefootAV

73 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: Orthobroker

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5404020402anklefootAV
Device name: Ankle Stirrup-Junior Air
Device model: 11-0003-JA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 29, 2022

Manufacturer & authorised representative

Manufacturer

Name: Orthobroker
SRN: BE-MF-000000331
Country: Belgium
Email: info@orthobroker.com
Phone: +3233851075

Variants by status

UDI-DI variants

73 UDI-DI variants

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Applied filters

basicUdiUlid01GE43087G9ZD7NE7CBA8E69Q9

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

No registered UDI-DI variants for this device family.