Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Dexpure 45801-30 — 8 UDI-DI variants, MDR

MD Atlas
Honeywell Safety Products France SAS

Data from EUDAMED, last updated May 19, 2026

Dexpure 45801-30

36038345800121308C

8 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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 36038345800121308C
Device name: Dexpure 45801-30
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 2, 2022

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

8 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01GGSBKTM2FQHKFNV7RR1AZT75

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 801-2103603835706160
DexPure 801-2103603835706177
DexPure 801-2103603835706184
45 801-21 10XL03603835706191
DexPure 801-30 10-XL03603835705422
DexPure 801-30 7-S03603835705392
DexPure 801-30 8-M03603835705408
DexPure 801-30 9-L03603835705415