QUADROX-i Adult Microporous Membrane Oxygenator with or without Arterial Filter with BIOLINE Coating

FDA registration

Sterigenics Belgium Petit Rechain S.A.·1 product·🇧🇪 Belgium

QUADROX-I ADULT MICROPOROUS MEMBRANE OXYGENATOR WITH BIOLINE COATING, MODEL BEHMO70000,BEQ-HMO70000

FDA 510(k)

FDA Class 2 ·Cardiovascular

MEDI

FDA UDI

MEDI MANUFACTURING, INC.·04051526827837·***DISC*LEVAMED ANKLE SUPPORT BLACK I

MEDI

FDA UDI

MEDI MANUFACTURING, INC.·04051526827899·ACHIMED ACHILLES SUPP BLACK I

Buccal Tubes

FDA UDI

AMERICAN ORTHODONTICS CORPORATION·00190746083587·DB TUBE MAND MOLAR 022 INCONEL TQ=0 R=0 2MM

N/A

FDA UDI

BIOMET MICROFIXATION, INC·00841036030087·

Agility (0.16) Steerable Guidewires

FDA registration

Cerenovus, Inc.·1 product·🇺🇸 United States

Cardinal Health Costa Rica, S.A.

FDA registration

Cardinal Health Costa Rica, S.A.·1 product·🇨🇷 Costa Rica

Kendall SCD Express Foot Cuff

FDA registration

Covidien·1 product·🇺🇸 United States

Kendall SCD Controller Tubing Extension Assembly

FDA registration

Medtronic Engineering and Innovation Center (MEIC)·1 product·🇮🇳 India

Cardinal Health

FDA registration

Cardinal Health·1 product·🇺🇸 United States

Kendall SCD Express Sequential Compression System

FDA registration

CELESTICA de MONTERREY S.A. de C.V.·1 product·🇲🇽 Mexico

Cardinal Health K.K.

FDA registration

Cardinal Health K.K.·1 product·🇯🇵 Japan

Cardinal Health (Kenmex Medical Specialties)

FDA registration

Cardinal Health (Kenmex Medical Specialties)·1 product·🇲🇽 Mexico

Cardinal Health 200, LLC

FDA registration

Cardinal Health 200, LLC·1 product·🇺🇸 United States

Agility (0.16) Steerable Guidewires

FDA registration

Cerenovus, Inc.·1 product·🇺🇸 United States

Kendall SCD Express Foot Cuff

FDA registration

Covidien Medical Products (Shanghai) Manufacturing LLC·1 product·🇨🇳 China

Oxygenator, Cardiopulmonary Bypass

FDA classification

FDA Class 2 ·Oxygenator, Cardiopulmonary Bypass

X-TIP

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

MODIFICATION TO: AGILITY STEERABLE GUIDEWIRES

FDA 510(k)

FDA Class 2 ·Cardiovascular