- Role
- Country
- Date of registration
- Address
CN-MF-000046524No 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.C-Reactive Protein/Serum Amyloid A (CRP/SAA) Test Kit (Immunofluorescence) is an IVDD-legacy in vitro diagnostic registered in EUDAMED. It is classified as IVDD — General. Manufactured by Shenzhen Huiyan Sci-Tech Biotechnology Co., Ltd.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Apr 10, 2026
B-06978198482134Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)06978198482134
1 warning recorded — scroll inside the panel to see all entries.
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.
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.
Primary placement in Germany; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | — | Still on market |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
06978198482134Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
B-069781984821342213UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
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.
European Medical Device Nomenclature — the EU product classification assigned to this device.
W01021199RHEUMATOID / INFLAMMATORY DISEASE MARKERS - OTHERNo certificate specifically references this device's Basic UDI-DI.
B-06978198482264On the marketAnti-Müllerian Hormone (AMH) Test Kit (Immunofluorescence)B-06978198482202On the marketC-Reactive protein (CRP) Test Kit (Immunofluorescence)B-06978198482141On the marketCreatine Kinase-MB (CK-MB) Test Kit (Immunofluorescence)B-06978198482226On the marketCreatine Kinase-MB / High-sensitivity Cardiac Troponin I / Myoglobin ( CK-MB/Hs-cTnI/Myo) Test Kit (Immunofluorescence)B-06978198482097On the marketD-Dimer Test Kit (Immunofluorescence)B-06978198482127On the market