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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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Armis™ Ankle — 6 UDI-DI variants, MDR (Mediroyal Nordic AB)

MD Atlas
Mediroyal Nordic AB

Data from EUDAMED, last updated May 31, 2026

Armis™ Ankle

73400329MBA1413Y

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: Mediroyal Nordic AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 73400329MBA1413Y
Device name: Armis™ Ankle
Device model: MBA141
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: Mediroyal Nordic AB
SRN: SE-MF-000007821
Country: Sweden
Email: lars.engstrand@mediroyal.se
Phone: +46709153270

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KRGEGM3DYYW398C7393HFKYF

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

Armis™ Ankle L07340032914689
Armis™ Ankle M07340032914672
Armis™ Ankle S07340032914665
Armis™ Ankle XL07340032914696
Armis™ Ankle XS07340032914658
Armis™ Ankle XXL07340032914702