37 results · 21ms · Sources: EU EUDAMED, US FDA

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RANDOX COMPLEMENT C4

FDA 510(k)
FDA Class 2 ·Immunology

Preat

FDA UDI
Preat Corporation·00842092169568·ASC NobelBiocare™ Tri-Lobe-compatible NP X 9mm ...

TEWA

FDA UDI
asia-med Gesellschaft für Akupunkturbedarf mbH & Co. KG·04251282503192·TeWa CJ-Type 3013 (s): uncoated acupuncture ne...

TEWA

FDA UDI
asia-med GmbH·04251282510510·TeWa CJ-Type 3013 (s): uncoated acupuncture ne...

Zavation

FDA UDI
Zavation LLC·00842166122154·4-Level, 68mm Cervical Plate

CURE ACP

FDA UDI
SpineArt SA·07640270065632·ANTERIOR CERVICAL PLATE, 4 LEVELS L68

PenEvac1

FDA UDI
I.C. MEDICAL, INC.·00817688020165·

CURE™ ACP

FDA UDI
MEDITECH SPINE, LLC·B167700004680·

GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 3/12 MM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·February 17, 2022

COMPUMEDICS E-SERIES EEG SYSTEM

FDA 510(k)
FDA Class 2 ·Neurology

CS/3 CRITICAL CARE MONITOR WITH S-ICU99(A)

FDA 510(k)
FDA Class 2 ·Cardiovascular

ENDOSCOPIC CO2 REGULATION UNIT

FDA Adverse Event
Injury ·SHIRAKAWA OLYMPUS CO., LTD.·Product code HIF·November 22, 2024

CURE 2.0 ACP

FDA UDI
SpineArt SA·07640375231628·CERVICAL 4 LEVEL TEMPLATE L68

CURE™ ACP

FDA UDI
MEDITECH SPINE, LLC·B167S1700004680·

CURE 2.0 ACP

FDA UDI
SpineArt SA·07640375234049·ANTERIOR CERVICAL PLATE, 4 LEVELS L68

CURE ACP

FDA UDI
SpineArt SA·07640270066141·ANTERIOR CERVICAL PLATE, 4 LEVELS L68

PWRD ECH FLEX 60MM

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·March 12, 2013

SHUNT SENSOR SYS500

FDA Adverse Event
TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code DRY·February 14, 2011

PULSE GEN MODEL 102

FDA Adverse Event
Injury ·CYBERONICS, INC.·Product code LYJ·February 21, 2008

BAXJECT II HI-FLOW NEEDLESS TRANSFER DEVICE

FDA Adverse Event
Malfunction ·TAKEDA PHARMACEUTICALS U.S.A., INC.·Product code LHI·May 4, 2026