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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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Dexpure 4580091 — 4 UDI-DI variants, MDR

MD Atlas
Honeywell Safety Products France SAS

Data from EUDAMED, last updated May 19, 2026

Dexpure 4580091

3603834580091XU

4 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: Honeywell Safety Products France SAS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3603834580091XU
Device name: Dexpure 4580091
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 5, 2023

Manufacturer & authorised representative

Manufacturer

Name: Honeywell Safety Products France SAS
SRN: FR-MF-000023170
Country: France
Email: markus.weber@kcl.de
Phone: +491704588043

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01GZNAG39AT3AP3XJHPG13D7VJ

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

DexPure 800-9103603835706245
DexPure 800-91 10-XL03603835706276
DexPure 800-91 8-M03603835706252
DexPure 800-91 9-L03603835706269