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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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STABILO G3 M — 2 UDI-DI variants, MDR (ORTOSERVIS s.r.o.)

MD Atlas
ORTOSERVIS s.r.o.

Data from EUDAMED, last updated May 23, 2026

STABILO G3 M

859420944005JV

2 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: ORTOSERVIS s.r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 859420944005JV
Device name: STABILO G3 M
Device model: STABILO G3 M
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: ORTOSERVIS s.r.o.
SRN: CZ-MF-000003866
Country: Czechia
Email: ortoservis@ortoservis.cz
Phone: +420 266 313 652

Variants by status

UDI-DI variants

2 UDI-DI variants

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basicUdiUlid01KS31R71ZRTNC7MC706TXVKJ9

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

2053508594209440085
2053408594209440078