Acuson Sequoia

FDA registration

ADVANCED ULTRASOUND ELECTRONICS·3 products·🇺🇸 United States

SEQUOIA SIGNATURE II DIAGNOSTIC ULTRASOUND SYSTEM

FDA 510(k)

FDA Class 2 ·Radiology

INSTANT-VIEW FSH Dip-Strip Test

FDA UDI

ALFA SCIENTIFIC DESIGNS, INC.·10796918000146·INSTANT-VIEW FSH Dip-Strip Test

StimuCath (19 Ga)

FDA registration

Arrow International, LLC (subsidiary of Teleflex Incorporated)·1 product·🇺🇸 United States

StimuCath (19 Ga)

FDA registration

Arrow International LLC (subsidiary of Teleflex Incorporated)·1 product·🇺🇸 United States

StimuCath (19 Ga)

FDA registration

Teleflex LLC (NADC 2)·1 product·🇺🇸 United States

Peregrine3901 (PL) - Keratome (Microkeratome) Blade

FDA registration

Isomedix Operations Inc.·1 product·🇺🇸 United States

StimuCath (19 Ga)

FDA registration

Arrow International CR, a.s.·1 product·🇨🇿 Czechia

Arrow Select Kits

FDA registration

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

MORIA S.A.

FDA registration

MORIA S.A.·1 product·🇫🇷 France

StimuCath (19 Ga)

FDA registration

Arrow Internacional de Chihuahua S.A. de C.V.·1 product·🇲🇽 Mexico

STERIS AST CZ s.r.o.

FDA registration

STERIS AST CZ s.r.o.·1 product·🇨🇿 Czechia

STERISERVICES

FDA registration

STERISERVICES·1 product·🇫🇷 France

StimuCath (19 Ga)

FDA registration

Arrow International C.R. a.s.·1 product·🇨🇿 Czechia

Moria S.A

FDA registration

Moria S.A·1 product·🇫🇷 France

Wondfo T-Dip Multi-Drug Urine Test Panel

FDA registration

WONDFO USA CO., LTD.·11 products·🇺🇸 United States

MODIFICATION TO: REAADS ANTI-PHOSPHATIDYLSERINE IGG/IGM SEMI-QUANTITATIVE TEST KIT

FDA 510(k)

FDA Class 2 ·Immunology

AKUPORT M1

FDA 510(k)

FDA Class 2 ·Neurology

Device, Galvanic Skin Response Measurement

FDA classification

FDA Class 2 ·Device, Galvanic Skin Response Measurement

System, Imaging, Pulsed Doppler, Ultrasonic

FDA classification

FDA Class 2 ·System, Imaging, Pulsed Doppler, Ultrasonic