76 results · 20ms · Sources: EU EUDAMED, US FDA

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Monitor, Uterine Contraction, External (For Use In Clinic)

FDA Pre-Market Approval
FDA Class 2 ·GENESIS(R) HOME UTERINE ACTIVITY MONITORING SYSTEM

Monitor, Uterine Contraction, External (For Use In Clinic)

FDA Pre-Market Approval
FDA Class 2 ·GENESIS SYSTEM & TERM GUARD I & TERM GUARD II SYS.

Monitor, Uterine Contraction, External (For Use In Clinic)

FDA Pre-Market Approval
FDA Class 2 ·GENESIS SYSTEM & TERM GUARD I & TERM GUARD II SYS.

Monitor, Uterine Contraction, External (For Use In Clinic)

FDA Pre-Market Approval
FDA Class 2 ·GENESIS HOME UTERINE ACTIVITY MONITORING SYSTEM (HUAM)

MYCARELINK

FDA Adverse Event
Malfunction ·PLEXUS MANUFACTURING SDN. BHD·Product code NVZ·May 3, 2018

MYCARELINK

FDA Adverse Event
Malfunction ·PLEXUS MANUFACTURING SDN. BHD·Product code NVZ·May 3, 2018

MYCARELINK

FDA Adverse Event
Malfunction ·PLEXUS MANUFACTURING SDN. BHD·Product code NVZ·June 15, 2018

UNKNOWN DEPUY TIBIAL TRAY

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.1818910·Product code JWH·June 24, 2014

LTV

FDA Adverse Event
Injury ·CAREFUSION 203, INC.·Product code CBK·October 28, 2010

DURATA STS OPTIM ACTIVE FIXATION

FDA Adverse Event
Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·December 28, 2012

Lens, Contact (Polymethylmethacrylate)

FDA Pre-Market Approval
FDA Unclassified ·PARAPERM O2 (PASIFOCON A) RGP CONTACT LENS

Lens, Contact (Polymethylmethacrylate)

FDA Pre-Market Approval
FDA Unclassified ·PARAPERM O2 CONTACT LENS

Lens, Contact (Polymethylmethacrylate)

FDA Pre-Market Approval
FDA Unclassified ·PARAPERM O2 CONTACT LENS

Lens, Contact (Polymethylmethacrylate)

FDA Pre-Market Approval
FDA Unclassified ·PARAPERM O2 CONTACT LENS

System, Test, Carcinoembryonic Antigen

FDA Pre-Market Approval
FDA Class 2 ·CEA-ROCHE TEST KIT

Lens, Contact (Polymethylmethacrylate)

FDA Pre-Market Approval
FDA Unclassified ·PARAPERM O2 CONTACT LENS

Lens, Contact (Polymethylmethacrylate)

FDA Pre-Market Approval
FDA Unclassified ·PARAPERM O2 (PASIFOCON A) CONTACT LENS

System, Test, Carcinoembryonic Antigen

FDA Pre-Market Approval
FDA Class 2 ·CEA-ROCHE TEST KIT

System, Test, Carcinoembryonic Antigen

FDA Pre-Market Approval
FDA Class 2 ·CEA-ROCHE TEST KIT

Lens, Contact (Polymethylmethacrylate)

FDA Pre-Market Approval
FDA Unclassified ·PARAPERM O2 CONTACT LENS