15 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ANOSPEC DISPOSABLE ANSOSCOPE WITH LIGHT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772813841·GENUMEDI PRO SILVER SIZE IV
Tasso+ Convenience Kit
FDA UDI
Tasso Inc.·00860006434557·Tasso+ convenience kit allows self-collection o...
UniTip Catheter
FDA UDI
Unisensor AG·07640172973226·
MAYFIELD RADIOLUCENT SKULL PINS, MODEL 4-0-A-2020
FDA 510(k)
FDA Class 2
·Neurology
VSI MICRO-INTRODUCER SETS (REGULAR, STIFFEN), MODELS 7197V-7209V, 7240V-7256V, 7259V, 7230V, 7231V, 7260V, 7274V
FDA 510(k)
FDA Class 2
·Cardiovascular
BD BACTEC; LYTIC/10 ANAEROBIC/F CULTURE VIALS
FDA Adverse Event
Malfunction
·BECTON DICKINSON CARIBE LTD.·Product code MDB·February 22, 2021
Ascendant
FDA UDI
Choice Spine, LP·10885862261021·
HEARTMATE II LVAS, EUROPE
FDA Adverse Event
Injury
·THORATEC CORP.·Product code DSQ·May 16, 2013
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·September 26, 2014
ASR UNI FEMORAL IMPL SIZE 46
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 2, 2011
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·August 12, 2016
THINFLAP SYSTEM CROSS-DRIVE, SELF-DRILLING SCREW 1.5X4MM
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code GWO·April 16, 2018
Cook brand Keller-Timmermans Introducer Set, straight with Rutner adapter includes: sheath 18.0 FR, 85 cm long without wire guide; VSSW-18.0-38-85-0-KTI.
FDA Recall
Terminated
·Cook, Inc.·Product code MIH·June 10, 2004
Artis Q biplane, Model Number 10848282
FDA Enforcement
Class II
·Ongoing·Siemens Medical Solutions USA, Inc·April 27, 2022