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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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TRINITY — 5 UDI-DI variants, MDR (KOELIS)

MD Atlas
KOELIS

Data from EUDAMED, last updated May 19, 2026

TRINITY

3665134TRINITY_01PL

5 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: KOELIS

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 3665134TRINITY_01PL
Device name: TRINITY
Device model: TRINITY
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: KOELIS
SRN: FR-MF-000000830
Country: France
Email: info@koelis.com

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KPWZNPRN9DD9JVN6NAK9V2TV

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

2D Abdominal probe03665134000097
K2DLN0003665134000103
K3DEC00-203665134000073
K3DEL0003665134000080
KURO-3000-303665134000684