- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on May 11, 2026
B-06974566303414Filariasis IgG/IgM Rapid Test is an IVDD-legacy in vitro diagnostic registered in EUDAMED. It is classified as IVDD — General. Manufactured by Zhuhai Encode Medical Engineering Co., Ltd.. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06974566303414IFI-422(01)06974566303414
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0103020803D-DIMER - RT & POCCN-MF-000019361No 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.Primary placement in France; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | May 26, 2022 | Dec 30, 2027 |
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 →B-06974566302684On the marketfFN Rapid TestB-06974566302745On the marketfFN Rapid TestB-06974566302714On the marketFlu A&B/ Covid-19/ RSV/ Adenovirus /MP Antigen Rapid Test PanelB-06974566303407On the marketFOB Rapid TestB-06974566303391On the marketFSH Menopause Rapid TestB-06974566303902On the marketNo certificate specifically references this device's Basic UDI-DI.