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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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KANGURO — 63 UDI-DI variants, MDR

MD Atlas
FABRICACIONES ORTOPEDICAS ALBACETE, S.L.

Data from EUDAMED, last updated May 23, 2026

KANGURO

84356695010VM

63 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: FABRICACIONES ORTOPEDICAS ALBACETE, S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84356695010VM
Device name: KANGURO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 10, 2026

Manufacturer & authorised representative

Manufacturer

Name: FABRICACIONES ORTOPEDICAS ALBACETE, S.L.
SRN: ES-MF-000004660
Country: Spain
Email: logistica@fortasl.es
Phone: +34967210313

Variants by status

UDI-DI variants

63 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KNW2Z2M96YZ20Q4S7J8BWG5Q

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

47200400408435669515626
47200401008435669518306
47200400708435669518276
47200400308435669515619
47200400608435669515640
47200401208435669518320
47200400908435669518290
47200500108435669515657
47200500308435669515671
47200500508435669518337
47200500608435669518344
47200500208435669515664
47200500408435669515688

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