DRAINAGE CATHETER OR FOLEY CATHETER

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

OIS SYMPHONY IMAGE MANAGMENT SYSTEM

FDA 510(k)

FDA Class 2 ·Radiology

Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

FDA Pre-Market Approval

FDA Class 3 ·Thoraflex™ Hybrid

CSM part #s: C210-006, C210-005, C210-018, C210-009, C220-028, C220-036, C220-041

FDA registration

MIDWEST STERILIZATION CORP.·1 product·🇺🇸 United States

Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

FDA Pre-Market Approval

FDA Class 3 ·Thoraflex Hybrid

Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

FDA Pre-Market Approval

FDA Class 3 ·Thoraflex™ Hybrid

Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

FDA Pre-Market Approval

FDA Class 3 ·Thoraflex™ Hybrid

Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

FDA Pre-Market Approval

FDA Class 3 ·Thoraflex™ Hybrid

Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

FDA Pre-Market Approval

FDA Class 3 ·Thoraflex Hybrid

Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

FDA Pre-Market Approval

FDA Class 3 ·Thoraflex Hybrid

Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

FDA Pre-Market Approval

FDA Class 3 ·Thoraflex™ Hybrid

Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

FDA Pre-Market Approval

FDA Class 3 ·Thoraflex™ Hybrid

Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

FDA Pre-Market Approval

FDA Class 3 ·Thoraflex Hybrid

Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

FDA Pre-Market Approval

FDA Class 3 ·Thoraflex™ Hybrid

PERSONA™

FDA UDI

Zimmer, Inc.·00889024239807·

PERSONA™

FDA UDI

Zimmer, Inc.·00889024239784·

PERSONA®

FDA UDI

Zimmer, Inc.·00889024642140·

PERSONA™

FDA UDI

Zimmer, Inc.·00889024239791·

PERSONA®

FDA UDI

Zimmer, Inc.·00889024642126·

PERSONA®

FDA UDI

Zimmer, Inc.·00889024642102·