Flow Cytometry catalog - ROW 2019

Regulatory Status

Status Definitions:

ASR

Analyte Specific Reagents (ASR)

An ASR is the active ingredient of an in-house (“home-brew”) test. It is the responsibility of the laboratory using the ASR to develop the test and to take responsibility for establishing and maintaining performance. These reagents are labeled “Analyte Specific Reagents. Analytical and performance characteristics are not established.” ASR are manufactured under GMP to ensure high consistency and are considered as Medical Devices and can be used for Diagnostics only in the USA.

CE

CE-marked products (CE)

CE marking on products included in this catalog indicates conformity to the legal requirements of the European Union (EU) Directive 98/79/EC of the European Parliament for in vitro diagnostic medical devices with respect to safety, health, environment, and consumer protection. In this catalog, CE-marked products are labeled for in vitro diagnostic use and can be traded freely throughout the EU.

In Vitro Diagnostic Products (IVD)

IVD

Reagents, instruments and systems intended for use in the diagnosis of disease or other conditions, including a determination of the state of health, in order to cure, mitigate, treat or prevent diseases. Such products are intended for use in the collection, preparation and examination of specimens taken from the human body. These products can be used for clinical diagnosis. These products are labeled “For In Vitro Diagnostic Use.”

IVD & CE

In Vitro Diagnostic Products & CE-Marked Products (IVD & CE)

These reagents comply with the IVD and CE classifications.

Laboratory Use Only Reagents (LUO)

LUO

Generic reagents whose use is generally known by a trained person. Not intended to identify a specific disease or condition. These reagents are labeled “For Laboratory Use Only.”

RUO

Research Use Only Reagents (RUO)

A product in the laboratory testing phase of development that does not have a recognized clinical utility and is not represented as an effective in vitro diagnostic product. These products cannot be used for clinical diagnosis, prognosis or therapeutic determinations. These reagents are labeled “For Research Use Only. Not for use in diagnostic procedures.”

nMD

Non-Medical Device (nMD) Equipment not intended to be used in diagnostic procedures.

Geographical Distribution:

CE-marked products are sold in European Union (EU) countries and are registered as clinical products in 30+ countries outside of Europe.

IVD products are sold in countries where they comply with applicable regulation.

INFORMATION

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Outside US Flow Cytometry Catalog