Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

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.

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

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

0601.180408435669518955
0601.176008435669513707
0601.190208436533438904
0601.190308436533438911
0601.201208435669511949
0601.201308435669511956
0601.201108435669511932
0601.201408435669511963
0601.202408435669519259
0601.201708435669511994
0601.202708435669519297
0601.190108436533438645
0601.190408436533438898
0601.190708436533438942
0601.038108435669514230
0601.150208436533436672
0601.150308436533436689
0601.150108436533436665
0601.150408436533436696
0601.150708436533436726
47200400208435669515602
47200400508435669515633
47200401108435669518313
47200400808435669518283
47200400108435669515596

1 2 3