- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Feb 6, 2023
5999862176BPackAcT-DiffT4BioPack AcT-Diff WBC-3-diff reagent is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Bioxol Kft. Placed on the EU market in Hungary. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
05999862176921CT-9011(01)05999862176921
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0103010105CBC-REAGENTS (CLEANING-/DILUTING-/LYSING-/SHEAT-FLUIDS)HU-MF-000025409The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Primary placement in Hungary; available across 1 country total.
Placed on the market in Hungary; per-country availability dates not published.
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
View in glossary →Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →IVDR risk classes
IVDR risk classes rank in-vitro diagnostic devices from lowest risk (Class A) to highest (Class D), based on the patient and public-health risk of a wrong result.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →No certificate specifically references this device's Basic UDI-DI.
No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.5999862176BioLyse-WHSYSGROn the marketBioLyse-WH SYS WBC-3-diff lysing reagent 1L5999862176BioLyse-WHSYSGROn the marketBioPack 5 WBC-5-diff reagent 1pack5999862176BioPack522On the marketBioPack WBC-3-diff reagent5999862176BioPackA6On the marketBioresh-SYS Cleaning reagent 1L5999862176Bioresh-SYSE3On the marketBioresh-SYS Cleaning reagent 5L5999862176Bioresh-SYSE3On the market