20 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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aeris Balloon Dialation Catheter
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
Oticon
FDA UDI
Oticon A/S·05707131283177·H11V2, MINIBTE 312 WL 85 CNB
Alleset
FDA UDI
GRI Medical & Electronic Technology Co., Ltd.·16931918159300·Sustainable Surgical Instrument Tray_Half Shall...
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100165·KRATZ-BARRAQUER SPECULUM SMALL
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100721·SMIRMAUL EYE SPECULUM WIRE
Alleset
FDA UDI
GRI Medical & Electronic Technology Co., Ltd.·16931918180779·Surgical Instrument Tray, Half Shallow_300ea/cs
Alleset
FDA UDI
GRI Medical & Electronic Technology Co., Ltd.·16931918115092·Surgical Instrument Tray_Half Shallow_Non-steri...
MEDTOX BUPRENORPHINE TEST
FDA 510(k)
FDA Class 2
·Clinical Toxicology
MEDSTAR 220, MODEL 533-220; MEDSTAR 230, MODEL 533-230; MEDSTAR 360, MODEL 533-360; MEDSTAR 370, MODEL 533-370
FDA 510(k)
FDA Class 2
·Cardiovascular
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·June 26, 2024
PORTABLE AIR COMPRESSOR FOR MEDICAL PURPOSES
FDA Adverse Event
Malfunction
·INVACARE SUZHOU·Product code BTI·June 6, 2013
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 21, 2011
HARMONIC ACE 36 CM
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code LFL·September 5, 2008
MREYE EMBOLIZATION COIL
FDA Adverse Event
Injury
·COOK INC·Product code KRD·May 11, 2018
MREYE EMBOLIZATION COIL
FDA Adverse Event
Injury
·COOK INC·Product code KRD·May 11, 2018
MREYE EMBOLIZATION COIL
FDA Adverse Event
Injury
·COOK INC·Product code KRD·May 11, 2018
NESTER PLATINUM EMBOLIZATION MICROCOIL
FDA Adverse Event
Injury
·COOK INC·Product code KRD·May 11, 2018
MREYE EMBOLIZATION COIL
FDA Adverse Event
Injury
·COOK INC·Product code KRD·May 11, 2018
MREYE EMBOLIZATION COIL
FDA Adverse Event
Injury
·COOK INC·Product code KRD·May 11, 2018
STAINLESS STEEL EMBOLIZATION COIL
FDA Adverse Event
Malfunction
·COOK INC·Product code KRD·August 24, 2017