LH Ovulation Test (Colloidal Gold)

Trade name

LH Ovulation Test (Colloidal Gold)

UDI-DI code

06952062770626

Basic UDI-DI

B-06952062770626

Reference / catalog number

LH2UST- 50

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

LH Ovulation Test (Colloidal Gold) is a qualitative test used to predict when there is a LH surge, and in turn, when you are likely to ovulate. LH Ovulation Test (Colloidal Gold) is used to detect the concentration of LH in urine in all levels of medical institutions and at home for self-testing.

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.

• W0102050105LUTEINISING HORMONE

3 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.

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