221 results · 95ms · Sources: EU EUDAMED, US FDA

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Core Products International, Inc.

Manufacturer
🇺🇸 United States·1 Importer

Core Products International Inc

FDA registration
Core Products International Inc·28 products·🇺🇸 United States

OmniMedical B.V.

Importer
🇳🇱 Netherlands·5 Manufacturers

PAB®

FDA Adverse Event
Malfunction ·B. BRAUN MEDICAL INC·Product code KPE·November 15, 2021

NOVOSYN VIOLET 3/0 (2) 70CM HR26 (M)

FDA Adverse Event
Malfunction ·B.BRAUN SURGICAL SA·Product code GAM·April 26, 2019

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·August 23, 2022

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·August 23, 2022

ECHOTIP PROCORE HIGH DEFINITION ULTRASOUND BIOPSY NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·August 24, 2022

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·August 24, 2022

GALAXY G3 XSFT 3MM X 4CM

FDA Adverse Event
Malfunction ·SEE H.10·Product code KRD·August 17, 2018

DAVINCI XI

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·March 5, 2026

DAVINCI SI

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·December 12, 2024

PINNACLE®

FDA Adverse Event
Malfunction ·B. BRAUN MEDICAL INC.·Product code KPE·July 17, 2019

GALAXY G3 3MM X 8CM

FDA Adverse Event
Malfunction ·REFER TO SECTION H10·Product code KRD·March 11, 2019

ARROW CVC SET: 3-LUMEN 7 FR X 16 CM

FDA Adverse Event
Malfunction ·ARROW INTERNATIONAL INC.·Product code DQY·December 29, 2020

PINNACLE®

FDA Adverse Event
Malfunction ·B. BRAUN MEDICAL INC.·Product code KPE·July 11, 2019

APEX¿

FDA Adverse Event
Malfunction ·B. BRAUN AVITUM ITALY S.P.A.·Product code KPE·June 4, 2019

APEX¿

FDA Adverse Event
Malfunction ·B. BRAUN AVITUM ITALY S.P.A.·Product code KPE·June 4, 2019

APEX¿

FDA Adverse Event
Malfunction ·B. BRAUN AVITUM ITALY S.P.A.·Product code KPE·June 4, 2019

APEX¿

FDA Adverse Event
Malfunction ·B. BRAUN AVITUM ITALY S.P.A.·Product code KPE·June 4, 2019