Sklar®

FDA UDI

SKLAR CORPORATION·10649111007071·COVER ONLY

OQW / 2009 h1n1 influenza virus (swine origin), nucleic acid or antigen, detection and identification

FDA registration

MONOCENT INC.·1 product·🇺🇸 United States

24-7Labs Corp

FDA registration

247LABKIT·1 product·🇺🇸 United States

Contract Manufactured Collection Device with Ahlstrom 226 filter paper.

FDA registration

Revvity Health Sciences, Inc.·1 product·🇺🇸 United States

Accurian™

FDA registration

RBC Development LLC dba RBC Medical Innovations dba Vantage MedTech·1 product·🇺🇸 United States

Trial Procedure Kit

FDA UDI

MEDIVATORS INC.·00677964084850·Trial Procedure Kit

Portex

FDA UDI

Smiths Medical ASD, Inc.·15019517078763·

Trial Procedure Kit

FDA UDI

MEDIVATORS INC.·00677964084843·Trial Procedure Kit

TRILLIUM MYOTHERM XP CARDIOPLEGIA DELIVERY SYSTEM, MODELS 41, 41-B

FDA 510(k)

FDA Class 2 ·Cardiovascular

SYNTHES CERVIFIX SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

Widex

FDA UDI

Widex A/S·05706069727104·Widex EVOKE E-PA (Titanium grey S-330 ) RC coil

Arthroscope

FDA classification

FDA Class 2 ·Arthroscope

Reservoir, Blood, Cardiopulmonary Bypass

FDA classification

FDA Class 2 ·Reservoir, Blood, Cardiopulmonary Bypass

Appliance, Fixation, Spinal Intervertebral Body

FDA classification

FDA Class 2 ·Appliance, Fixation, Spinal Intervertebral Body