Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·Evera MRI DF-1 ICD, Evera MRI ICD, Evera S DR ICD, Evera S VR ICD, Evera XT DR ICD, Evera XT VR ICD, Mirro MRI DR ICD, M

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·Evera MRI DF-1 ICD, Evera MRI ICD, Evera S DR ICD, Evera S VR ICD, Evera XT DR ICD, Evera XT VR ICD, Mirro MRI DR ICD, M

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·Evera MRI DF-1 ICD, Evera MRI ICD, Evera S DR ICD, Evera S VR ICD, Evera XT DR ICD, Evera XT VR ICD, Mirro MRI DR ICD, M

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·Evera MRI DF-1 ICD, Evera MRI ICD, Evera S DR ICD, Evera S VR ICD, Evera XT DR ICD, Evera XT VR ICD, Mirro MRI DR ICD, M

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·Evera MRI DF-1 ICD, Evera MRI ICD, Evera S DR ICD, Evera S VR ICD, Evera XT DR ICD, Evera XT VR ICD, Mirro MRI DR ICD, M

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·Evera MRI DF-1 ICD, Evera MRI ICD, Evera S DR ICD, Evera S VR ICD, Evera XT DR ICD, Evera XT VR ICD, Mirro MRI DR ICD, M

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·Evera MRI DF-1 ICD, Evera MRI ICD, Evera S DR ICD, Evera S VR ICD, Evera XT DR ICD, Evera XT VR ICD, Mirro MRI DR ICD, M

72-00174-0 S & N HOSE & DIN ASSEMBL

FDA registration

Northgate Technologies Inc.·1 product·🇺🇸 United States

Herpes Simplex IgM Control

FDA UDI

Bion Enterprises, Ltd.·B110HSM35300·

Oral B Pro Health Clinical Pro Flex.

FDA registration

MAPAEX HEALTH AND PERSONALCARE IRELAND PRIVATE LIMITED·1 product·🇮🇪 Ireland

OLYMPUS NEUROSCOPE, MODELS S-1349/1, S-1349/2, S-1349/3 AND S-1349/4

FDA 510(k)

FDA Class 2 ·Neurology

OSSIOfiber® Hammertoe Fixation System

FDA UDI

OSSIO LTD·07290017630076·The OSSIOfiber® Hammertoe Fixation System, S, ...

OSSIOfiber® Hammertoe Fixation System

FDA UDI

OSSIO LTD·07290017630090·The OSSIOfiber® Hammertoe Fixation System, M, ...

AKAS MEDICAL EQUIPMENT

Manufacturer

🇮🇳 India·5 Basic UDI-DIs·5 Devices·INSTITUT PRO TESTOVÁNI A CERTIFIKACI, a. s. (INSTITUTE FOR TESTING AND CERTIFICATION) merged with ex-NB 1390 and INSTITUT PRO TESTOVÁNI A CERTIFIKACI, a. s. (INSTITUTE FOR TESTING AND CERTIFICATION) merged with ex-NB 1390

Curaplex

FDA UDI

BOUND TREE MEDICAL, LLC·00810071636660·LARYN.BLADE,MAC 0,S/S,ENGLISH

BJ3603-II-45

FDA registration

SHANGHAI BOJIN ELECTRIC INSTRUMENT & DEVICE CO.,LTD.·1 product·🇨🇳 China

COBAS INTEGRA REAGENT CASSETTES

FDA registration

ROCHE DIAGNOSTICS GMBH·5 products·🇩🇪 Germany

Positive Lupus Anticoagulant Plasma

FDA registration

GEORGE KING BIO-MEDICAL, INC.·1 product·🇺🇸 United States

NEXUS MEDICAL, LLC

FDA registration

NEXUS MEDICAL, LLC·1 product·🇺🇸 United States

Preferred Plus

FDA registration

SCOTT SPECIALTIES, INC.·1 product·🇺🇸 United States