12 results
·
23ms
·
Sources: EU EUDAMED, US FDA
PULMONARY FUNCTION TESTER, COMPUTERIZED
FDA 510(k)
FDA Class 2
·Anesthesiology
NA
FDA UDI
Zimmer, Inc.·00889024132993·
NA
FDA UDI
Zimmer, Inc.·00889024132979·
NA
FDA UDI
Zimmer, Inc.·00889024132986·
NA
FDA UDI
Zimmer, Inc.·00889024133006·
NA
FDA UDI
Zimmer, Inc.·00889024133013·
RAZOR, DISPOSABLE
FDA 510(k)MPS ACACIA ENTERAL FEEDING TUBE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
TRI-LOCK BPS SZ 3 HI OFFSET
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code KWA·October 10, 2012
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP.·Product code FRN·December 3, 2013
FEMORAL RASP SIZE 2.5
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS MAHWAH·Product code LXH·July 26, 2010
Promote, Sterile EO, Model #/ Part #: 3207-30/60010740-207, 60010740-407; 3207-36/60010743-207, 60010743-407; 3213-36/50022126-001, 60013879-307, 60013879-407, 60013879-707; CD3211-36/100006984,100012548, 100012550, 100016680, 100031621, 100035618, 100035619, 100042487, 100047194; CD3211-36Q/100004091, 100004093,100019784, 100035620, 100042486, 100047054; CD3215-36/100006995, 100010246, 100010247, 100010249, 100010250, 100012569, 100012570, 100034981, 100046577, 100046802, 60019065; CD3215-36Q/100004059, 100004060, 100004061, 100023304, 100030590, 100033678, 100042492, 100046803, 100046906
FDA Enforcement
Class II
·Terminated·St Jude Medical Inc.·July 4, 2018