REPAIR DEVICE

FDA registration

BIOMET, INC.·1 product·🇺🇸 United States

Maxfire MarXmen

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

MAXFIRE MARXMEN MENISCAL REPAIR DEVICE

FDA 510(k)

FDA Class 2 ·Orthopedic

989803183101 989803183101

FDA registration

Philips Electronics Ltd·1 product·🇨🇦 Canada

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

FDA registration

MONOCENT INC.·1 product·🇺🇸 United States

989803183101 989803183101

FDA registration

Philips North America LLC·1 product·🇺🇸 United States

NEOLEADS

FDA registration

NEOTECH PRODUCTS, LLC·1 product·🇺🇸 United States

ORTA MEDICAL LTD

FDA registration

ORTA MEDICAL LTD·1 product·🇮🇱 Israel

NEONATAL ECG ELECTRODE

FDA registration

R & D MEDICAL PRODUCTS, INC.·1 product·🇺🇸 United States

989803183101 989803183101

FDA registration

Philips North America LLC·1 product·🇺🇸 United States

Custom Procedure Kit

FDA UDI

MEDIVATORS INC.·00677964111327·Custom Procedure Kit

Chartis Console

FDA registration

PULMONX, Corp.·1 product·🇺🇸 United States

Abacus 3CP Hematology Analyzer

FDA registration

Diatron MI Plc·1 product·🇭🇺 Hungary

NEOLEAD

FDA 510(k)

FDA Class 2 ·Cardiovascular

CDC INFLUENZA 2009 A(H1N1)PDM REAL-TIME RT-PCR PANEL

FDA 510(k)

FDA Class 2 ·Microbiology

Fastener, Fixation, Nondegradable, Soft Tissue

FDA classification

FDA Class 2 ·Fastener, Fixation, Nondegradable, Soft Tissue

2009 H1n1 Influenza Virus (Swine Origin), Nucleic Acid Or Antigen, Detection And Identification

FDA classification

FDA Class 2 ·2009 H1n1 Influenza Virus (Swine Origin), Nucleic Acid Or Antigen, Detection And Identification

Electrode, Electrocardiograph

FDA classification

FDA Class 2 ·Electrode, Electrocardiograph