Arrow Select Kits

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

Arrow-Clarke Pleura-Seal Thoracentesis Kit

FDA registration

Arrow International, LLC (subsidiary of Teleflex Incorporated)·1 product·🇺🇸 United States

Arrow-Clarke Pleura-Seal Thoracentesis Kit

FDA registration

Teleflex LLC (NADC 2)·1 product·🇺🇸 United States

Arrow-Clarke Pleura-Seal Thoracentesis Kit

FDA registration

Arrow Internacional de Chihuahua S.A. de C.V.·1 product·🇲🇽 Mexico

Arrow Select Kits

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

Arrow-Clarke Pleura-Seal Thoracentesis Kit

FDA registration

Teleflex Medical de Mexico, S. de R.L. de C.V.·1 product·🇲🇽 Mexico

Arrow-Clarke Pleura-Seal Thoracentesis Kit

FDA registration

Teleflex LLC (NADC)·1 product·🇺🇸 United States

ARROW-CLARKE(TM) PLEURA-SEAL(TM) THORACENTESIS KIT

FDA 510(k)

FDA Class 2 ·General Hospital

Catheter And Tip, Suction

FDA classification

FDA Class 2 ·Catheter And Tip, Suction

GC Initial™

FDA UDI

Gc America Inc.·J0228705721·GC Initial™ MC Translucent TN, 50g

GC Initial™

FDA UDI

Gc America Inc.·15400556703257·GC Initial™ MC Translucent TN, 50g

Yellowstone Interbody Fusion System

FDA registration

Pantheon Spinal LLC·1 product·🇺🇸 United States

G7540, Pointe Glycohemoglobin Reagent

FDA registration

HORIBA INSTRUMENTS INCORPORATED·1 product·🇺🇸 United States

PLIF Peek Implant

FDA registration

AR FABRICATING·1 product·🇺🇸 United States

Isomedix Operations, Inc.

FDA registration

Isomedix Operations, Inc.·1 product·🇺🇸 United States

Greatbatch Medical

FDA registration

Greatbatch Medical·1 product·🇺🇸 United States

Summit Spine Yellowstone Lumbar Interbody Fusion System

FDA 510(k)

FDA Class 2 ·Orthopedic

ASH ADVANCE HEMODIALYSIS CATHETER AND PROCEDURE KIT, MODELS; 15FR X 24CM, 15FR X 28CM, 15FR X 32CM

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

Catheter, Hemodialysis, Implanted

FDA classification

FDA Class 2 ·Catheter, Hemodialysis, Implanted

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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