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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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GIEMSA STAIN — 5 UDI-DI variants, IVDR (QUIMICA CLINICA APLICADA S.A.)

MD Atlas
QUIMICA CLINICA APLICADA S.A.

Data from EUDAMED, last updated May 23, 2026

GIEMSA STAIN

8430155GIEMSARC

5 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: QUIMICA CLINICA APLICADA S.A.

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 8430155GIEMSARC
Device name: GIEMSA STAIN
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jan 11, 2024

Manufacturer & authorised representative

Manufacturer

Name: QUIMICA CLINICA APLICADA S.A.
SRN: ES-MF-000001512
Country: Spain
Email: rtec@qca.es
Phone: +34977701439

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HKW94D8ZBAF1KRKF3D2TZB4K

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

Giemsa (1 x 1000 mL)08430155004547
99570508430155008750
99844008430155005230
99430518430155009969
Phosphate Buffer - giemsa,pH 7.2 (8 x 25 mL)18430155008252