Rapid fFN® Control Kit (Rapid fFN® for the TLI IQ® System).

TLI IQ® QCette®

System that detects fFN in cervicovaginal secretions.

FDA Product Code, Supplement Authorization and FDA Listing Number are not required for BLA products.

FDA Product Code, Supplement Authorization and FDA Listing Number are not required for BLA products.

FDA Product Code, Supplement Authorization and FDA Listing Number are not required for BLA products.

FDA Product Code, Supplement Authorization and FDA Listing Number are not required for BLA products.

Processes liquid based cytologic specimens to produce a uniform layer of cells on a glass microsope slide.

For use with the ThinPrep® system to preserve gynecological specimens.

Processes liquid based cytologic specimens to produce a uniform layer of cells on a glass microsope slide.

A system for imaging and analyzing ThinPrep® cervical cyctology sample slides.

A system for imaging and analyzing ThinPrep® cervical cyctology sample slides.

A microscope used to screen ThinPrep® pap test slides that have been imaged by a ThinPrep® Image Processor.

Computer to operate the ThinPrep® Imaging System.

Computer to operate the ThinPrep® Imaging System.

System that detects fFN in cervicovaginal secretions.

Server for use with the ThinPrep® Imaging System to enable review.

Computer to operate the ThinPrep® Imaging System.

Computer to operate the ThinPrep® Integrated Imager and Review Scope Manual+.

Computer to operate the ThinPrep® Integrated Imager and Review Scope Manual+.

A system for imaging and analyzing ThinPrep® cervical cyctology sample slides.

An automated microscope used to screen ThinPrep® pap test slides that have been imaged by a ThinPrep® Image Processor.

Computer to operate the ThinPrep® Integrated Imager and Review Scope Manual+.

Computer to operate the ThinPrep® Imaging System.

Server for use with the ThinPrep® Imaging System to enable review.

Server for use with the ThinPrep® Imaging System to enable review.

Computer to operate the ThinPrep® Imaging System.

The NovaSure® Impedance Controlled Endometrial Ablation System is intended to ablate the endometrial lining of the uterus in pre-menopausal women with menorrhagia (excessive bleeding) due to benign causes for whom childbearing is complete.

The NovaSure® Impedance Controlled Endometrial Ablation System is intended to ablate the endometrial lining of the uterus in pre-menopausal women with menorrhagia (excessive bleeding) due to benign causes for whom childbearing is complete.

The NovaSure® Impedance Controlled Endometrial Ablation System is intended to ablate the endometrial lining of the uterus in pre-menopausal women with menorrhagia (excessive bleeding) due to benign causes for whom childbearing is complete.

The NovaSure® Impedance Controlled Endometrial Ablation System is intended to ablate the endometrial lining of the uterus in pre-menopausal women with menorrhagia (excessive bleeding) due to benign causes for whom childbearing is complete.

The NovaSure®Impedance Controlled Endometrial Ablation System is intended to ablate the endometrial lining of the uterus in pre-menopausal women with menorrhagia (excessive bleeding) due to benign causes for whom childbearing is complete.