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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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THETIS — 11 UDI-DI variants, MDR (IMPLANTS SERVICE ORTHOPEDIE)

MD Atlas
IMPLANTS SERVICE ORTHOPEDIE

Data from EUDAMED, last updated May 19, 2026

THETIS

3615570THETISXG

11 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: IMPLANTS SERVICE ORTHOPEDIE

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3615570THETISXG
Device name: THETIS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 6, 2024

Manufacturer & authorised representative

Manufacturer

Name: IMPLANTS SERVICE ORTHOPEDIE
SRN: FR-MF-000000297
Country: France
Email: durier@evolutis-group.com
Phone: +33169021920

Variants by status

UDI-DI variants

11 UDI-DI variants

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Applied filters

basicUdiUlid01HNZJB09M3FF8F6870NJZ9AWS

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

THETIS03615570002360
THETIS03615570002353
THETIS03615570002377
THETIS03615570002339
THETIS03615570002414
THETIS03615570002391
THETIS03615570002438
THETIS03615570002421
THETIS03615570002346
THETIS03615570002407
THETIS03615570002384