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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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DEHYDRANT — 6 UDI-DI variants, IVDR (LAURYPATH)

MD Atlas
LAURYPATH

Data from EUDAMED, last updated May 19, 2026

DEHYDRANT

37015164ETHANOLGJ

6 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: 37015164ETHANOLGJ
Device name: DEHYDRANT
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jul 3, 2024

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

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J1VS4P4FJJBFTKEFNHG12TEJ

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

70% Dehydrant03701516402070
95% Dehydrant03701516402087
Dehydrant, Isopropyl Alcohol 4x5L03701516402131
Denatured Absolute Alcohol03701516402094
Syntri Safeguard Dehydrant, Isopropyl Alcohol 4x5L03701516402124
Syntri SafeguardTM Denatured Absoltue Alcohol03701516402063