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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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Yumizen H1500 — 4 UDI-DI variants, IVDR (HORIBA ABX SAS)

MD Atlas
HORIBA ABX SAS

Data from EUDAMED, last updated May 19, 2026

Yumizen H1500

361023ymz_h1500JQ

4 UDI-DI variants

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

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Manufacturer: HORIBA ABX SAS

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Device characteristics

Professional testing

Clinical investigations

Investigation number: Not available
Registered: No
Countries: United States

Registered: No

Identity & classification

Basic UDI-DI: 361023ymz_h1500JQ
Device name: Yumizen H1500
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Version date: Oct 16, 2023

Manufacturer & authorised representative

Manufacturer

Name: HORIBA ABX SAS
SRN: FR-MF-000000320
Country: France
Email: caroline.ferrer@horiba.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HCW6HVA7R92T4QHV2TYHTV5F

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

1300031324, 1300031325, 1300046881, 130004688403610230008591
1300031324, 1300031325, 1300046881, 1300046884 03610230008188
130010214503610230009420
130010214603610230009437