68 results · 22ms · Sources: EU EUDAMED, 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