SafeBreak Vascular

FDA registration

LINEUS MEDICAL·1 product·🇺🇸 United States

SafeBreak Vascular

FDA 510(k)

FDA Class 2 ·General Hospital

Intravenous Catheter Force-Activated Separation Device.

FDA classification

FDA Class 2 ·Intravenous Catheter Force-Activated Separation Device.

SYNTHES ANTERIOR TENSION BAND (ATB) SYSTEM; K022791

FDA registration

EXEL INC. DBA DHL SUPPLY CHAIN (USA)·1 product·🇺🇸 United States

BD Difco™ Salmonella H Antiserum z10

FDA UDI

BECTON, DICKINSON AND COMPANY·00382902227915·BD Difco™ Salmonella H Antiserum z10

AESCULAP AG

FDA registration

AESCULAP AG·1 product·🇩🇪 Germany

Jabil Inc. (Brandywine)

FDA registration

Jabil Inc. (Brandywine)·1 product·🇺🇸 United States

SYNTHES ANTERIOR TENSION BAND (ATB) SYSTEM

FDA registration

Synthes (USA) Products LLC·1 product·🇺🇸 United States

SYNTHES ANTERIOR TENSION BAND (ATB)

FDA registration

Synthes GMBH·1 product·🇨🇭 Switzerland

SYNTHES ANTERIOR TENSION BAND (ATB)

FDA registration

DEPUY ORTHOPAEDICS·1 product·🇺🇸 United States

Jabil Inc. (Elmira)

FDA registration

Jabil Inc. (Elmira)·1 product·🇺🇸 United States

SYNTHES ANTERIOR TENSION BAND (ATB)

FDA registration

SYNTHES GMBH·1 product·🇨🇭 Switzerland

Lyoplant Onlay

FDA registration

HA2 MEDIZINTECHNIK GMBH·1 product·🇩🇪 Germany

AESCULAP, INC.

FDA registration

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

Jabil Switzerland Manufacturing GmbH (Raron)

FDA registration

Jabil Switzerland Manufacturing GmbH (Raron)·1 product·🇨🇭 Switzerland

Access Intact PTH (P/N: A16972 MN and IE MFG)

FDA registration

Beckman Coulter Ireland Inc·1 product·🇮🇪 Ireland

SYNTHES ANTERIOR TENSION BAND (ATB) SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

LYOPLANT ONLAY

FDA 510(k)

FDA Class 2 ·Neurology

Dura Substitute

FDA classification

FDA Class 2 ·Dura Substitute

Appliance, Fixation, Spinal Intervertebral Body

FDA classification

FDA Class 2 ·Appliance, Fixation, Spinal Intervertebral Body