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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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GPS Ankle — 2 UDI-DI variants, MDR (Blue Ortho SAS)

MD Atlas
Blue Ortho SAS

Data from EUDAMED, last updated May 19, 2026

GPS Ankle

3770041302GPSANKLENA

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Blue Ortho SAS

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 3770041302GPSANKLENA
Device name: GPS Ankle
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Mar 25, 2026

Manufacturer & authorised representative

Manufacturer

Name: Blue Ortho SAS
SRN: FR-MF-000002436
Country: France
Email: info@blue-ortho.com
Phone: 0458003525

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KMJ68S5NMWJX2G29N6K64MM0

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

L0048103770041302179
L0048003770041302162