22 results
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42ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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APD LUER-LOCK ADAPTER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MAX-TI HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304225268·
CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 24mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665033557·
Diversatek Healthcare
FDA UDI
DIVERSATEK HEALTHCARE, INC.·M7831240240·Straight Thoracic Catheter, 24 French x 20 IN
Alltest Multi-Drug 13 Drugs Rapid Urine Test Panel
FDA UDI
Hangzhou AllTest Biotech Co., Ltd.·16936983179642·25T, FDA CLIA WAIVED, white package, MOP(OPI)30...
MiniSPC Button
FDA UDI
APPLIED MEDICAL TECHNOLOGY, INC.·00842071152369·12F x 4.0cm MiniSPC Low Profile Suprapubic Cath...
Segmental Plating System
FDA UDI
ALPHATEC SPINE, INC.·00190376545752·SPS VA Self-Drill Screw, 4.0 x 24mm
Atoll™
FDA UDI
Seaspine Orthopedics Corporation·10889981052553·4.0mm x 24mm Poly Screw Assm. The Atoll OCT Spi...
Sochi
FDA UDI
Altus Spine, LLC·00843210166667·Polyaxial Screw, 4.0mm x 24mm
Insignia
FDA UDI
ALPHATEC SPINE, INC.·00190376329994·4.0mm Variable Angle, Self-Drilling Screw, Sing...
Proximity
FDA UDI
ALPHATEC SPINE, INC.·00190376694863·PROXIMITY VA SELF-DRILL SCREW, 4.0 x 24mm
MECTALIF TRANSFORAMINAL
FDA 510(k)
FDA Class 2
·Orthopedic
MEDSOURCE IV ADMINSTRATION SET
FDA 510(k)
FDA Class 2
·General Hospital
MECTALIF ANTERIOR STAND-ALONE PLATE FLUSH H.12 MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code OVD·March 29, 2018
CN LOCK SCREW, F THREAD, Ø4.0MM X 24MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code KTW·June 12, 2024
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Injury
·ANIMAS CORPORATION·Product code LZG·May 22, 2013
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·September 27, 2014
MAXIMO VR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code LWS·June 14, 2011
SPECTRA WAVEWRITER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·November 10, 2019
ALIF SCREWDRIVER UNIVERSAL JOINT
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code LXH·January 15, 2016