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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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CLEARANT — 2 UDI-DI variants, IVDR (LAURYPATH)

MD Atlas
LAURYPATH

Data from EUDAMED, last updated May 19, 2026

CLEARANT

37015164XYLENEQ6

2 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: LAURYPATH

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Device characteristics

Reagent

Identity & classification

Basic UDI-DI: 37015164XYLENEQ6
Device name: CLEARANT
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Oct 14, 2025

Manufacturer & authorised representative

Manufacturer

Name: LAURYPATH
SRN: FR-MF-000020948
Country: France
Email: contact@laurypath.fr
Phone: +33 4 78 34 21 67

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01K7GRWKFZ6V5BSMX1MTH8RWMG

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

Syntri Safeguard Xylene03701516402117
Xylene03701516402100