38 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ANTI-HAV
FDA 510(k)
FDA Class 2
·Microbiology
Premier
FDA UDI
PREMIER DENTAL PRODUCTS COMPANY·00856402006313·Decan Stopper Size 6 Closure Full
Endo Carry-On Procedure Kit
FDA UDI
MEDIVATORS INC.·40677964017535·Endo Carry-on Procedure Kit includes tray and ...
Tasso+ Convenience Kit
FDA UDI
Tasso Inc.·00850038691035·
Copper Ni-Ti - Archwire
FDA UDI
ORMCO CORPORATION·00889989027341·COPPER NITI 27 BAF 17X25U/S PK10
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450196571·
Mariner MIS
FDA UDI
Seaspine Orthopedics Corporation·10889981294960·Modular Handle, Large
Life Instruments
FDA UDI
Life Instrument Corporation·M930810090300·Brun Curette #3 Str
Life Instruments
FDA UDI
Life Instrument Corporation·M930810090310·Brun Curette #3 Ang
Life Instruments
FDA UDI
Life Instrument Corporation·M930810090320·Brun Curette #3 Rev Ang
ALEUTIAN® Interbody Systems
FDA UDI
VB Spine LLC·10888857527850·AN Lordotic Spreader Size 8.5x24x4 mm, 12°
ADDITIONAL ASSAYS FOR BAYER ADVIA IMS SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Toxicology
TRI-FIX SPINAL FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Life Instruments
FDA UDI
Life Instrument Corporation·M9308100903210·Custom Brun Rev. Ang. #3 60 deg (C1973-08)
TUBE CEV649-5B DIA 5MM 350MM
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INSTRUMENTATION S.A.S. LE PAVILLON·Product code GEI·August 29, 2013
LEEP PRECISION GENERATOR
FDA Adverse Event
Malfunction
·COOPERSURGICAL, INC.·Product code HGI·September 22, 2023
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 8, 2013
MEDTRONIC ATTAIN ABILITY 4196
FDA Adverse Event
Injury
·MEDTRONIC, INC·Product code OJX·May 18, 2011
PROXIMATE ILS CURVED CIR STAPL
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, LLC·Product code GDW·August 6, 2008
ADULT DUAL HEATED BREATHING CIRCUIT
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·April 29, 2012