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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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Advita GPS — 18 UDI-DI variants, MDR (Blue Ortho SAS)

MD Atlas
Blue Ortho SAS

Data from EUDAMED, last updated May 19, 2026

Advita GPS

3770041302ADVITAGPS2G

18 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: 3770041302ADVITAGPS2G
Device name: Advita GPS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 17, 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

18 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KPD9VCCJ690351BHNG1T29GG

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

J0012003770041302216
A1000303770041302117
A0020303770041302070
J0001003770041302186
J0001103770041302193
J0006503770041302209
I0002203770041302056
I0002103770041302049
I0002510885862574091
I0003203770041302025
I0003003770041302001
I0003103770041302018
A1000403770041302124
A0020403770041302087
A0020603770041302100
A1000603770041302148
A0020503770041302094
A1000503770041302131