72 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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V. Mueller
FDA UDI
STERIS CORPORATION·10885403279249·V. Mueller DISPOSABLE BIPOLAR FORCEPS
RIS500
FDA 510(k)
FDA Class 2
·Radiology
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756614320·Knee Immobilizer
BONE PIN, 3.2MM X 140MM, STERILE 2 PACK
FDA Adverse Event
Injury
·MAKO SURGICAL CORP.·Product code OLO·June 26, 2017
BONE PIN, 3.2MM X 140MM, STERILE 2 PACK
FDA Adverse Event
Injury
·MAKO SURGICAL CORP.·Product code OLO·June 26, 2017
ELMED
FDA UDI
ELMED INCORPORATED·00198506057052·ELLIK EVACUATOR - STANDARD CONE CONNECTOR
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756885935·KNEE IMMOBILIZER, TRI-PANEL
I/A HANDPIECE, 21G ANGLED 45°
FDA UDI
Carl Zeiss Meditec AG·04049539100252·This single use device is an accessory for ZEIS...
SureCore Semi-automatic Disposable Biopsy Needle
FDA UDI
Canyon Medical Inc.·06954414658392·Semi-automatic Disposable Biopsy Needle
BONE PIN, 3.2MM X 140MM, STERILE 2 PACK
FDA Adverse Event
Malfunction
·MAKO SURGICAL CORP.·Product code OLO·August 15, 2018
Electro Lavage
FDA UDI
MECTRA LABS, INC.·00817984010594·Electro Lavage Needle Double Bottle
BONE PIN, 3.2MM X 110MM, STERILE 2 PACK
FDA Adverse Event
Injury
·MAKO SURGICAL CORP.·Product code OLO·May 9, 2017
BONE PIN, 3.2MM X 110MM, STERILE 2 PACK
FDA Adverse Event
Injury
·MAKO SURGICAL CORP.·Product code OLO·April 21, 2017
BONE PIN, 3.2MM X 110MM, STERILE 2 PACK
FDA Adverse Event
Injury
·MAKO SURGICAL CORP.·Product code OLO·April 17, 2017
BONE PIN, 3.2MM X 110MM, STERILE 2 PACK
FDA Adverse Event
Injury
·MAKO SURGICAL CORP.·Product code OLO·April 17, 2017
SureCore Semi-automatic Disposable Biopsy Needle
FDA UDI
Canyon Medical Inc.·06954414658439·Semi-automatic Disposable Biopsy Needle
SureCore Semi-automatic Disposable Biopsy Needle
FDA UDI
Canyon Medical Inc.·06954414658415·Semi-automatic Disposable Biopsy Needle
SMART READ BIOLOGICAL TEST PACK
FDA 510(k)
FDA Class 2
·General Hospital
MODIFICATION TO D-TRONPLUS
FDA 510(k)
FDA Class 2
·General Hospital
MAYFIELD MODIFIED SKULL CLAMP
FDA Adverse Event
Injury
·INTEGRA LIFESCIENCES CORPORATION·Product code HBL·May 30, 2013