ARROW

FDA UDI

TELEFLEX INCORPORATED·00801902077882·Radial Arterial Catheterization Kit

ARROW

FDA UDI

TELEFLEX INCORPORATED·10801902117660·Arterial Catheterization Kit

UNO 30

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

UNO Negative Pressure Wound Therapy System

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

UNO Negative Pressure Wound Therapy System

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

PATIENT EXAMINATION GLOVES

FDA 510(k)

FDA Class 1 ·General Hospital

PATIENT EXAMINATION GLOVES (LATEX)

FDA 510(k)

FDA Class 1 ·General Hospital

NATURAL RUBBER LATEX MALE CONDOMS

FDA 510(k)

FDA Class 2 ·Obstetrics/Gynecology

MALE LATEX CONDOM (STRAIGHT SIDE OR CONTOURED OR FLARED IN SHAPE, EITHER TEXTURED OR NON-TEXTURED , LUBRICATED OR NON-LU

FDA 510(k)

FDA Class 2 ·Obstetrics/Gynecology

Quantum Mitohormesis (QMT) (M2101)

FDA 510(k)

FDA Class 2 ·Physical Medicine

LATEX EXAMINATION GLOVES

FDA 510(k)

FDA Class 1 ·General Hospital

RUBBER CONTRACEPTIVE

FDA 510(k)

FDA Class 2 ·Obstetrics/Gynecology

Genadyne DUO NPWT

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Defibrillator, Implantable, Dual-Chamber

FDA Pre-Market Approval

FDA Class 3 ·PHYLAX AV ICD SYSTEM

Defibrillator, Implantable, Dual-Chamber

FDA Pre-Market Approval

FDA Class 3 ·KRONOS LV-T CRT-D

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·PHYLAX IMPLANTABLE CARDIOVERTER DIFIBRILLATOR

Pulse Generator, Permanent, Implantable

FDA Pre-Market Approval

FDA Class 3 ·DROMOS DR/DR-A AND DROMOS SR/SR-B CARDIAC

MANUKAhd wound dressings

FDA registration

ManukaMed Limited Partnership·1 product·🇳🇿 New Zealand

ManukaMed Limited Partnership

FDA registration

ManukaMed Limited Partnership·1 product·🇳🇿 New Zealand

MANUKAtex wound dressings

FDA registration

ManukaMed Limited Partnership·1 product·🇳🇿 New Zealand