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MICROPORE INC

FDA registration
MICROPORE INC·1 product·🇺🇸 United States

SpiraLith Ca

FDA UDI
Micropore, Inc.·00860008449832·

SpiraLith Ca

FDA UDI
Micropore, Inc.·00860008449825·

SpiraLith Ca

FDA UDI
Micropore, Inc.·00860008449849·

SpiraLith Ca

FDA UDI
Micropore, Inc.·00860008449870·

VECTRA VASCULAR ACCESS GRAFT (D: 5MM, L: 40CM)

FDA Adverse Event
Malfunction ·THORATEC CORPORATION·Product code DSY·January 7, 2022

SURGICEL ABSORBABLE HEMOSTAT UNKNOWN

FDA Adverse Event
Injury ·ETHICON INC.·Product code LMG·September 14, 2021

PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAW·September 20, 2023

SECURESTRAP UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GDW·August 18, 2022

MONOSYN QUI UNDY 3/0 (2) 70CM HR22(M)

FDA Adverse Event
Malfunction ·B.BRAUN SURGICAL SA·Product code GAM·December 16, 2016

INTROCAN

FDA Adverse Event
Injury ·B. BRAUN MELSUNGEN AG·Product code DQR·September 17, 2021

640G INSULIN PUMP MMT-1711K

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 10, 2018

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code MEA·August 11, 2025

Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as Primary PLUM Set Yellow Striped Tubing, Distal Microbore Tubing, 0.2 Micron Filter, Secure Lock, 107 Inch. 1 unit per pouch; 48 pouches per case

FDA Recall
Terminated ·ICU Medical Inc·Product code FRN·July 29, 2019

Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Epidural Set Yellow-Striped Microbore, 0.2 Micron Filter 119 Inch. 1 unit per pouch; 50 pouches per case

FDA Recall
Terminated ·ICU Medical Inc·Product code FRN·July 29, 2019

Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Epidural Set Yellow-Striped Microbore, 0.2 Micron Filter 301 cm / 8.3 mL. 1 unit per blister; 40 blisters per case . Not distributed in the U.S.

FDA Recall
Terminated ·ICU Medical Inc·Product code FRN·July 29, 2019

Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Primary 1.2 Micron Filter Set Microbore, 122 Inch. 1 unit per pouch; 50 pouches per case

FDA Recall
Terminated ·ICU Medical Inc·Product code FRN·July 29, 2019

Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Epidural Set Yellow-Striped Microbore, 0.2 Micron Filter, PAV 123 inch. 1 unit per pouch; 50 pouches per case

FDA Recall
Terminated ·ICU Medical Inc·Product code FRN·July 29, 2019

Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Primary 0.2 Micron Filter Set, Microbore, CLAVE Y-Site, 118 Inch. 1 unit per pouch; 50 pouches per case

FDA Recall
Terminated ·ICU Medical Inc·Product code MRZ·July 29, 2019

Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Primary 0.2 Micron Filter Set Non-Vented, Microbore, PAV, CLAVE Y-Site, 122 Inch. 1 unit per pouch; 50 pouches per case

FDA Recall
Terminated ·ICU Medical Inc·Product code FRN·July 29, 2019