cleanser, root canal Straumann Pref Gel 0.6 ml

FDA registration

Sterigenics Radiation Technologies, LLC·1 product·🇺🇸 United States

Straumann® PrefGel

FDA registration

INSTITUT STRAUMANN AG·1 product·🇨🇭 Switzerland

Straumann® PrefGel

FDA registration

BIORA AB·1 product·🇸🇪 Sweden

STRAUMANN PREFGEL

FDA 510(k)

FDA Unclassified ·Unknown

Cleanser, Root Canal

FDA classification

FDA Unclassified ·Cleanser, Root Canal

ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

FDA UDI

FX SOLUTIONS·03701037312858·STD TRIAL CUP FOR BOACH Ø36+12

PowerLoc Safety Infusion Set

FDA registration

Integra Biotechnical, SA de CV·2 products·🇲🇽 Mexico

Titanium PowerPort

FDA registration

BARD REYNOSA S.A. DE C.V.·2 products·🇲🇽 Mexico

PowerLoc Safety Infusion Set

FDA registration

FOREFRONT MEDICAL TECHNOLOGY (PTE) LTD.·2 products·🇸🇬 Singapore

MALLEABLE TUNNELER, SINGLE BARB, 8 FR

FDA registration

TURNXON PRECISION CO., LTD·1 product·🇨🇳 China

NESSY Omega Return Electrodes

FDA registration

ERBE ELEKTROMEDIZIN GMBH·1 product·🇩🇪 Germany

PowerLoc Safety Infusion Set

FDA registration

Grupo American Industries, S.A. De C.V·2 products·🇲🇽 Mexico

Titanium PowerPort

FDA registration

C.R. BARD, INC.·2 products·🇺🇸 United States

PowerLoc Safety Infusion Set

FDA registration

FOREFRONT MEDICAL TECHNOLOGY (JIANGSU) CO.,LTD·2 products·🇨🇳 China

Titanium PowerPort

FDA registration

Bard Access Systems, Inc.·2 products·🇺🇸 United States

Titanium PowerPort

FDA registration

C.R. BARD, INC.·2 products·🇺🇸 United States

ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

FDA UDI

FX SOLUTIONS·03701037317518·STANDARD TRIAL FIXED CUP FOR BROACH Ø36 +12

Atlantis SR Pro 40 MHz Coronary Imaging Catheter

FDA registration

Sterigenics US LLC·2 products·🇺🇸 United States

VACUETTE SPEEDY QUICK-RELEASE HOLDER

FDA 510(k)

FDA Class 2 ·General Hospital

SPIROLAB II, MODEL 29

FDA 510(k)

FDA Class 2 ·Anesthesiology