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EUDAMED last updated this device on May 29, 2026
8905459HEMANA3KMerilyzer CelQuant 5 is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Meril Diagnostics Pvt. Ltd.. Placed on the EU market in Bulgaria. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
18906074562026HMFCLQ-01(01)18906074562026
European Medical Device Nomenclature — the EU product classification assigned to this device.
W02020199CELL COUNTING INSTRUMENTS - OTHERPrimary placement in Bulgaria; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| BulgariaPrimary placement | — | Still on market |
IN-MF-000028158The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
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 →8905459FABA75On the marketMerilyzer CelQuant 3608905459HEMANA3KOn the marketMerilyzer CelQuant 3i8905459HEMANA3KOn the marketMerilyzer CelQuant 5 Plus8905459HEMANA3KOn the marketMerilyzer CelQuant 5 Ultima8905459HEMANA3KOn the marketMerilyzer CelQuant 5 Ultima8905459HEMANA3KOn the marketCertificate health across this manufacturer's portfolio.
2024-IVDR/TD-010/AAmendedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
2023-IVDR/QS-004/BAmendedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
2024-IVDR/TD-009AmendedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
2025-IVDR/QS-001/AAmendedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
2024-IVDR/QS-010/AAmendedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
2024-IVDR/QS-003/AAmendedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →No certificate specifically references this device's Basic UDI-DI.