55 results · 21ms · Sources: EU EUDAMED, US FDA

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MOSS MIAMI 6.35MM ROD SYSTEM MONOAXIAL SCREWS, POLYAXIAL REDUCTION SCREWS AND SACRAL EXTENDERS

FDA 510(k)
FDA Class 2 ·Orthopedic

MICRO PULL THRU CASSETTE REFILL (360X12)

FDA UDI
MEDIVATORS INC.·40677964021778·MICRO PULL THRU CASSETTE REFILL (360X12)

ADVANCE®

FDA UDI
Microport Orthopedics Inc.·M684K00126071·

GRADIA®

FDA UDI
Gc America Inc.·D0470026071·GRADIA® DIRECT X Syringes - 1 syringe 2.7 mL/5 ...

GRADIA®

FDA UDI
Gc America Inc.·14548161292238·GRADIA® DIRECT X Syringes - 1 syringe 2.7 mL/5 ...

Battalion

FDA UDI
ALPHATEC SPINE, INC.·00840967189000·Battalion, LLIF Trial, 0°, 26 mm Wide, 07 mm X ...

SOLO-CARE BRAND HARD SOLUTION

FDA 510(k)
FDA Class 2 ·Ophthalmic

REPROBEAD T3 ENZYME IMMUNOASSAY REAGENT KIT (CATALOG# 104)

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

STEM: AMISTEM-P COLLARED AMISTEM-P COLLARED STD STEM SIZE 1

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·June 1, 2021

SYNCHRO GUIDEWIRE

FDA Adverse Event
Malfunction ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORPORATION·Product code DQX·July 9, 2009

SYNCHRO GUIDEWIRE

FDA Adverse Event
Malfunction ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORPORATION·Product code DQX·July 9, 2009

SYNCHRO GUIDEWIRE

FDA Adverse Event
Malfunction ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORP.·Product code DQX·September 4, 2009

SYNCHRO GUIDEWIRE

FDA Adverse Event
Malfunction ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORP.·Product code DQX·September 4, 2009

SYNCHRO 14 NEURO GUIDEWIRE

FDA Adverse Event
Injury ·NEUROVASCULAR, A DIVISION OF BOSTON SCIENTIFIC CORPORATION·Product code DQX·July 24, 2007

SYNCHRO GUIDEWIRE

FDA Adverse Event
Malfunction ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORPORATION·Product code DQX·August 18, 2009

SYNCHRO -10 NEURO GUIDEWIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORP., NEUROVASCULAR DIV·Product code DQX·December 15, 2006

SYNCHRO-14 NEURO GUIDEWIRE

FDA Adverse Event
Malfunction ·NEUROVASCULAR , A DIV. OF BOSTON SCIENTIFIC CORP·Product code DQX·December 19, 2006

SYNCHRO 14 GUIDEWIRE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORP.·Product code DQX·September 20, 2007

SYNCHRO .014 GUIDEWIRE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORP. / NEUROCASCULAR DIVISION·Product code DQX·August 16, 2007

SYNCHRO .014 GUIDEWIRE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORP. / NEUROVASCULAR DIV.·Product code DQX·August 16, 2007