HMS Plus

Indications, Safety, and Warnings

ACT Plus^®

HMS Plus

ACT Plus

Contraindication: This device used for any other purposes than for the indicated use is the responsibility of the user.

Indication: The ACT Plus^® instrument is intended for in vitro diagnostic testing in either a hospital laboratory setting or a point of care (decentralized) setting (e.g., in the operating room, cardiac catheterization lab, intensive care unit, or clinic, etc.).

Warnings: Proper instrument and cartridge use. The instrument and cartridges must only be used in the manner and purpose for which they are intended. Instructions for proper use are included in the manual and in the cartridge insert package inserts. Read all warnings, precautions, and Instructions For Use carefully prior to use.

Caution: Federal law (USA) restricts this device to sale by or on the order of a physician. For a complete listing of indications, contraindications, precautions and warnings, please refer to the Instructions For Use which accompany each product.

HMS Plus

Contraindication: This device used for any other purposes than for the indicated use is the responsibility of the user.

Indication: The HMS Plus instrument is a microprocessor based, multichannel clot timing system with automated syringe handling for pipetting blood into single use cartridges. It performs in vitro heparin sensitivity evaluations, heparin assays, and activated clotting times.

Warnings: Proper instrument and cartridge use. The instrument and cartridges must only be used in the manner and purpose for which they are intended. Instructions for proper use are included in the manual and in the cartridge insert package inserts. Read all warnings, precautions, and Instructions For Use carefully prior to use.

Caution: Federal law (USA) restricts this device to sale by or on the order of a physician. For a complete listing of indications, contraindications, precautions and warnings, please refer to the Instructions For Use which accompany each product.