Kimberly-Clark Inc.

FDA registration

Kimberly-Clark Inc.·1 product·🇨🇦 Canada

U by Kotex

FDA registration

KIMBERLY-CLARK CORPORATION·1 product·🇺🇸 United States

U by Kotex

FDA registration

Kimberly-Clark Inc.·1 product·🇨🇦 Canada

Poise

FDA registration

Kimberly-Clark Corporation·1 product·🇺🇸 United States

U by Kotex

FDA registration

K-C AFC Manufacturing, S. de R.L. de C.V·1 product·🇲🇽 Mexico

LithoDiamond

FDA registration

HealthTronics, Inc·1 product·🇺🇸 United States

Brachytherapy Radionuclide

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

PedFuse®

FDA UDI

SPINEFRONTIER, INC.·00190361008767·PedFuse Respond, CNL, 9.0mm x 75mm

V11-3EUltrasonic Transducer(FDA)

FDA UDI

Shenzhen Mindray Bio-Medical Electronics Co., Ltd.·06944904087955·

SERAGARD VASCULAR ACCESS PATCH

FDA 510(k)

FDA Class 2 ·General Hospital

HEART 2005

FDA 510(k)

FDA Class 2 ·Cardiovascular

Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

FDA classification

FDA Class 2 ·Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

MaxTorque™

FDA UDI

TORNIER, INC.·00846832054237·

Transmitters And Receivers, Electrocardiograph, Telephone

FDA classification

FDA Class 2 ·Transmitters And Receivers, Electrocardiograph, Telephone

Needle, Hypodermic, Single Lumen

FDA classification

FDA Class 2 ·Needle, Hypodermic, Single Lumen