RUBELLA Quant IgG

FDA registration

SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED·1 product·🇬🇧 United Kingdom

RUBELLA Quant IgG

FDA registration

Siemens Healthcare Diagnostics Inc.·1 product·🇺🇸 United States

IMMULITE RUBELLA IGG

FDA 510(k)

FDA Class 2 ·Microbiology

Enzyme Linked Immunoabsorbent Assay, Rubella

FDA classification

FDA Class 2 ·Enzyme Linked Immunoabsorbent Assay, Rubella

Hypodermic Syringe Without Needle

FDA registration

Terumo Medical Canada, Inc.·1 product·🇨🇦 Canada

Bluephase Style 20i

FDA registration

IVOCLAR VIVADENT Manufacturing GmbH·1 product·🇦🇹 Austria

Terumo® Syringe Pharmacy Tray

FDA registration

TERUMO (PHILIPPINES) CORPORATION·1 product·🇵🇭 Philippines

Bluephase Style 20i

FDA registration

IVOCLAR VIVADENT, INC.·1 product·🇨🇦 Canada

Bluephase Style 20i

FDA registration

IVOCLAR VIVADENT AG·1 product·🇱🇮 Liechtenstein

Fiber Optic Rod

FDA registration

SCHOTT CR, S.R.O.·1 product·🇨🇿 Czechia

Bluephase Style 20i

FDA registration

Ivoclar Vivadent GmbH·1 product·🇩🇪 Germany

MODIFICATION TO TERUMO SYRINGE WITH/WITHOUT NEEDLE

FDA 510(k)

FDA Class 2 ·General Hospital

Bluephase Style 20i

FDA 510(k)

FDA Class 2 ·Dental

Activator, Ultraviolet, For Polymerization

FDA classification

FDA Class 2 ·Activator, Ultraviolet, For Polymerization

Syringe, Piston

FDA classification

FDA Class 2 ·Syringe, Piston