MAVEN Patient-Specific Instrumentation System

FDA registration

PARAGON 28·2 products·🇺🇸 United States

Maven Patient-Specific Instrumentation

FDA 510(k)

FDA Class 2 ·Orthopedic

Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer

FDA classification

FDA Class 2 ·Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer

Conventional Lead Apron .5mm Xtra Large 25 X 40

FDA UDI

Flow X Ray Corporation·00843696123628·Conventional Lead Apron .5mm Xtra Large 25 X 40...

10PW - General Purpose

FDA UDI

Certified Safety Manufacturing, Inc.·00766588020129·10PW - General Purpose

Corneal Trephine

FDA UDI

KATENA PRODUCTS, INC.·00841668112526·BARRON VACUUM TREPHINE 8.25MM

Retrograde Cardioplegia Cannula

FDA registration

Terumo BCT STERILIZATION SERVICES, Inc.·1 product·🇺🇸 United States

Perifix Catheter Connector

FDA registration

B. BRAUN MELSUNGEN AG·1 product·🇩🇪 Germany

Retrograde Cardioplegia Cannula

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

RAUMEDIC - Muenchberg

FDA registration

RAUMEDIC - Muenchberg·1 product·🇩🇪 Germany

Retrograde Cardioplegia Cannula

FDA registration

LivaNova USA, INC.·1 product·🇺🇸 United States

Corneal Trephine

FDA UDI

KATENA PRODUCTS, INC.·00841668112649·BARRON CORNEAL PUNCH 8.25MM

Genius AI Detection

FDA registration

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

LensHooke Semen Test Cassette CS0;LensHooke Semen Test Cassette CS1

FDA registration

BONRAYBIO USA CORPORATION·1 product·🇺🇸 United States

RETROGRADE CARDIOPLEGIA CANNULA, SELF-INFLATING, WITH MALLEABLE OR GUIDEWIRE STYLET

FDA 510(k)

FDA Class 2 ·Cardiovascular

PERIFIX CATHETER CONNECTOR

FDA 510(k)

FDA Class 2 ·Anesthesiology

Catheter, Conduction, Anesthetic

FDA classification

FDA Class 2 ·Catheter, Conduction, Anesthetic

Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

FDA classification

FDA Class 2 ·Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass