Schistosoma Antibody Test Kit(Serum/plasma/whole blood)

Trade name

Schistosoma Antibody Test Kit(Serum/plasma/whole blood)

UDI-DI code

86979834610047

Basic UDI-DI

B-86979834610047

Reference / catalog number

SEA0035

Issuing entity

GS1

Risk category

IVDD — General

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

Schistosoma antibody test kit is a rapid chromatographic immunoassay method used for qualitative detection of schistosome antibodies in serum/plasma/whole blood samples. Only for in vitro diagnostic use.

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

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

• W0105090499PARASITES - RT & POC - OTHER

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

• CW009

  EUDAMED did not publish a description for this code.
• CW022

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• CW020

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• CW218

  EUDAMED did not publish a description for this code.
• CW463

  EUDAMED did not publish a description for this code.
• CW018

  EUDAMED did not publish a description for this code.
• CW278

  EUDAMED did not publish a description for this code.
• CW010

  EUDAMED did not publish a description for this code.

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