34 results · 24ms · Sources: EU EUDAMED, US FDA

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PERLA® TL posterior osteosynthesis system

FDA 510(k)
FDA Class 2 ·Orthopedic

XLP - CPRotector® Deluxe - Orange Nylon Pouch

FDA UDI
Certified Safety Manufacturing, Inc.·00766588030067·XLP - CPRotector® Deluxe - Orange Nylon Pouch

16PW - Krispy Kreme FAK - Poly White

FDA UDI
Certified Safety Manufacturing, Inc.·00766588015064·16PW - Krispy Kreme FAK - Poly White

Oph. Cystotomes

FDA UDI
KATENA PRODUCTS, INC.·00841668113660·CYSTOTOME STRAIGHT 25GA

SURGICAL MEDICAL DEVICE CAUTERY

FDA 510(k)
FDA Class 2 ·Ophthalmic

1.5T HEAD COIL (HC150), 3T HEAD COIL (HC300)

FDA 510(k)
FDA Class 2 ·Radiology

BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX SYSTEM

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO.·Product code QJR·September 18, 2020

BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO.·Product code QJR·September 11, 2020

BD MAX SYSTEM, BD MAX INSTRUMENT

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO.·Product code OOI·September 3, 2020

RESTORE RECHARGEABLE NEUROSTIMULATOR

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO·Product code LGW·October 17, 2008

ADAPTA SR

FDA Adverse Event
Malfunction ·MEDTRONIC S.A.·Product code NVZ·August 11, 2011

ACCESS

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - MALTA·Product code FMG·July 2, 2013

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·July 7, 2022

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·September 9, 2022

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·July 8, 2022

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·July 8, 2022

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·July 8, 2022

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·July 8, 2022

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·August 17, 2022

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·September 1, 2022