Organization name

Nanjing Vazyme Medical Technology Co.,Ltd.

SRN

CN-MF-000031032

Manufacturer status

Active

4 warnings recorded — scroll inside the panel to see all entries.

• CW010

  EUDAMED did not publish a description for this code.
• CW009

  EUDAMED did not publish a description for this code.
• CW007

  EUDAMED did not publish a description for this code.
• CW032

  EUDAMED did not publish a description for this code.

Primary placement in Spain; available across 1 country total.

Trade name

Full-Scale C-Reactive Protein (CRP) Test Kit (Quantum Dots Fluorescence Immunochromatography)

UDI-DI code

Primary DI

The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.

06973315736886

Basic UDI-DI

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.

B-06973315736886

Reference / catalog number

C2402CV

Issuing entity

UDI issuing entities

Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.

GS1

Risk category

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.

IVDD — General

Applicable legislation

IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]

Status

On the market

Quantity

1

Additional product description

Full-Scale C-Reactive Protein (CRP) Test Kit (Quantum Dots Fluorescence Immunochromatography) is a quantitative in vitro diagnostic medical device for the detection of CRP in human serum, plasma, peripheral blood and whole blood by photometric measurement. Measurement of CRP is of use for the evaluation of inflammatory disorders and associated diseases, infection and tissue injury. The kit is intended for use by trained professionals in point-of-care settings such as pharmacies, physician offices, physician office laboratories, clinics and hospitals, and clinical laboratory settings.

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

European Medical Device Nomenclature — the EU product classification assigned to this device.

• W01021109C-REACTIVE PROTEIN

• IVDD — General medical devices in EUDAMED

Certificate health across this manufacturer's portfolio.

No certificate specifically references this device's Basic UDI-DI.