AESCULAP AG

FDA registration

AESCULAP AG·1 product·🇩🇪 Germany

AESCULAP CESPACE PEEK INTERVERTEBRAL BODY FUSION SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

Nutrisafe

FDA registration

VYGON S A·1 product·🇫🇷 France

PowerPort with Groshong Catheter

FDA registration

C.R. BARD, INC.·1 product·🇺🇸 United States

PowerPort with Groshong Catheter

FDA registration

BARD REYNOSA S.A. DE C.V.·1 product·🇲🇽 Mexico

Nutrisafe

FDA registration

Vygon Verneuil·1 product·🇫🇷 France

PowerPort with Groshong Catheter

FDA registration

C.R. BARD, INC.·1 product·🇺🇸 United States

PowerPort with Groshong Catheter

FDA registration

Bard Access Systems, Inc.·1 product·🇺🇸 United States

MALLEABLE TUNNELER, SINGLE BARB, 8 FR

FDA registration

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

Zavation

FDA UDI

ZAVATION LLC·00842166177321·Z-Link Lumbar Sizer 8 deg, 33mm x 11

Zavation

FDA UDI

ZAVATION LLC·00842166112308·Z-Link Lumbar Spacer 8deg 33mmx11

Anti-dsDNA-NcX ELISA (IgG)

FDA registration

EUROIMMUN US INC.·1 product·🇺🇸 United States

Anti-dsDNA-NcX ELISA (IgG)

FDA registration

EUROIMMUN Medizinische Labordiagnostika AG·1 product·🇩🇪 Germany

MODIFICATION TO: POCKETVIEW ECG SOFTWARE

FDA 510(k)

FDA Class 2 ·Cardiovascular

NUTRISAFE PUR ENTERAL FEEDING TUBE

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

Intervertebral Fusion Device With Bone Graft, Cervical

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Cervical

Tube, Feeding

FDA classification

FDA Class 2 ·Tube, Feeding

Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

FDA classification

FDA Class 2 ·Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)