68 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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C.A.T.S. CONTINUOUS AUTOTRANSFUSION SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
Corin TriFit CF Hip Stem
FDA UDI
CORIN LTD·05055343898314·TriFit™ CF Stem Standard Size 6
SIGMA
FDA UDI
DEPUY (IRELAND)·10603295231981·SIGMA FEMORAL CRUCIATE RETAINING CEMENTED 6 LEFT
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR89600061·Mand. 2. Molar band W-Fit left 06
Eye Shield
FDA UDI
KATENA PRODUCTS, INC.·00841668111123·FOX EYE SHIELD ALUMINUM
Nx Nail Instrument Kit
FDA UDI
Eca Medical Instruments·00857676008416·5.0 Nail
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR89600060101·Mand. 2. Molar band W-Fit left 06
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR89600060051·Mand. 2. Molar band W-Fit left 06
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR89600060501·Mand. 2. Molar band W-Fit left 06
Vit Kit-Freeze Oocytes, Embryos and PN zygotes Vitrification Freeze Kit, Vit Kit-Thaw Oocytes, Embryos and PN zygotes Vitrification Thaw Kit
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
BRAUN THERMOSCAN IRT 2000 INFRARED EAR THERMOMETER
FDA 510(k)
FDA Class 2
·General Hospital
SHIRLEY CUFFED TRACHEOSTOMY TUBE
FDA Adverse Event
Death
·MALLINCKRODT MEDICAL INC·Product code BTO·December 10, 1996
Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker Electrodes
FDA Pre-Market Approval
FDA Class 3
·SWEET TIP(R) RX STEROID ELUTING LEAD
MOTORIZED 3-WHEELED VEHICLE FOR OUTSIDE TRANSPORT
FDA Adverse Event
CHIEN TI ENTERPRISE CO. LTD·Product code INI·February 13, 2013
PRECISE PRO RX CAROTID STENT SYSTEM
FDA Adverse Event
Death
·CORDIS DE MEXICO·Product code NIM·January 13, 2011
LARGE CRANIOTOME, BM
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code GFF·December 13, 2013
Permanent Defibrillator Electrodes
FDA Pre-Market Approval
FDA Class 3
·FLEXTEND PACING LEADS
Permanent Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·FLEXTEND FAMILY OF PACING LEADS
Permanent Defibrillator Electrodes
FDA Pre-Market Approval
FDA Class 3
·SWEET TIP RX/FLEXTEND
Permanent Defibrillator Electrodes
FDA Pre-Market Approval
FDA Class 3
·FLEXTEND FAMILY OF LEADS