Progesterone（P）Detection Kit（Magnetic Solid Phase Chemiluminescent Immunoassay）

Trade name

Progesterone（P）Detection Kit（Magnetic Solid Phase Chemiluminescent Immunoassay）

UDI-DI code

06974969981097

Basic UDI-DI

B-06974969981097

Reference / catalog number

50 Tests/kit（DR1029-1）

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

This is used for quantitative in vitro detection of progesterone (P) content in human serum. Progesterone is the first bioactive steroid compound produced in the steroid biosynthesis pathway and can be synthesized and secreted by tissues such as the adrenal cortex, testes, and ovaries. Luteinizing hormone in the body can regulate the synthesis and secretion of progesterone and participate in the balance of steroid hormone metabolism and the regulation of endocrine homeostasis. Changes in progesterone levels can objectively reflect the synthesis and secretion functions of endocrine glands such as the adrenal and gonads, and can be used for auxiliary screening and differential diagnosis of diseases related to steroid metabolism disorders and endocrine dysfunction in the body. It provides laboratory reference basis for clinical assessment of endocrine function and disease monitoring.

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.

• W0102050106PROGESTERONE

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