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EUDAMED last updated this device on Apr 22, 2026
B-GKPD196Y5S100β Protein Detection Kit (Immunofluorescence Chromatography） is an IVDD-legacy in vitro diagnostic registered in EUDAMED. It is classified as IVDD — General. Manufactured by Dezhou Guoke Medical Technology Co., Ltd.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
CN-MF-000044128D-GKPD196Y5
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.
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CW010Sterile
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.
D-GKPD196Y5Basic 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-GKPD196Y5GKPD196UDI 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.
W01021702PROTEIN S-100 BPrimary 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.B-GKPD147XQOn the marketRSV Ag Detection Kit (Immunofluorescence Chromatography)B-GKPD151XFOn the marketRSV Antigen Rapid Test Cassette (ColloidalGold)B-06977698400563On the marketSalmonella Ag Rapid Test KitB-GKPD126XGOn the marketSARS-CoV-2 Ag Detection Kit (Immunofluorescence Chromatography)B-GKPD149XUOn the marketSARS-CoV-2 / Flu A / Flu B/ ADV Ag Combo Rapid Test KitB-GKPD107XCOn the market