BIOMONITOR III

FDA registration

BIOTRONIK SE & CO. KG·1 product·🇩🇪 Germany

BIOMONITOR III

FDA registration

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

BIOMONITOR IIIm, BIOMONITOR III

FDA 510(k)

FDA Class 2 ·Cardiovascular

Recorder, Event, Implantable Cardiac, (With Arrhythmia Detection)

FDA classification

FDA Class 2 ·Recorder, Event, Implantable Cardiac, (With Arrhythmia Detection)

Ultraverse 014 and 018 PTA Balloon Dilatation Catheters

FDA registration

CLEARSTREAM TECHNOLOGIES LTD.·1 product·🇮🇪 Ireland

Provicol QM Aesthetic

FDA registration

VOCO GMBH·1 product·🇩🇪 Germany

Ultraverse 014 and 018 PTA Balloon Dilatation Catheters

FDA registration

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

Ultraverse 014 and 018 PTA Balloon Dilatation Catheters

FDA registration

BARD PERIPHERAL VASCULAR, INC.·1 product·🇺🇸 United States

Ultraverse 014 and 018 PTA Balloon Dilatation Catheters

FDA registration

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

PINNACLE

FDA UDI

DEPUY (IRELAND)·10603295520573·PINNACLE DUAL MOBILITY LINER TRIAL 56/49

PORGES URETERAL CATHETERS, MODELS ACN6XX, ACN5XX, AC5B, AC5C07, ACP5XX, ACP2XX, ACP3XX, ACP4XX, ACP6XX

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

ULTRAVERSE 014 AND 018 PTA BALLOON DILATATION CATHETERS LINE EXTENSION

FDA 510(k)

FDA Class 2 ·Cardiovascular

Catheter, Ureteral, Gastro-Urology

FDA classification

FDA Class 2 ·Catheter, Ureteral, Gastro-Urology

Catheter, Angioplasty, Peripheral, Transluminal

FDA classification

FDA Class 2 ·Catheter, Angioplasty, Peripheral, Transluminal