2,480 results · 24ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

RayFlow

FDA 510(k)
FDA Class 2 ·Cardiovascular

NA

FDA UDI
Stryker GmbH·00886385008813·Titanium Ankle Fusion Nail, Left

Eye Wash Station - 16 Poly White

FDA UDI
Certified Safety Manufacturing, Inc.·00766588220239·Eye Wash Station - 16 Poly White

TruFit™

FDA UDI
Ortho Organizers, Inc.·00190707192006·TruFit 2.0 022 MC UL6/7 NC SBT -14T 10Off DB SB...

MIXJECT WITH SPRAY HEAD

FDA 510(k)
FDA Class 2 ·General Hospital

COMPASS ESOPHAGEAL PRESSURE CATHETER, MODEL GIE-8500, COMPASS ANO-RECTAL PRESSURE CATHETER, MODEL GIA-8500

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

PUMP MMT-1880L MM770G BLE MG

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·July 11, 2023

PUMP MMT-1714K 630G BLACK MMOL CANADA

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·August 11, 2023

MINIMED 770G US SYSTEM BLE CONNECT 3.0 MG/DL

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·June 15, 2023

MINIMED 780G OUS SYSTEM BLE CONNECT 3.0 MMOL/L

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·April 7, 2023

PRECISION

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·November 6, 2008

RESMED S8 SERIES

FDA Adverse Event
Injury ·RESMED INC·Product code BZD·August 18, 2011

TRANSTAR STRETCHER

FDA Adverse Event
Malfunction ·HILL-ROM, INC.·Product code FPO·July 3, 2013

PUMP MMT-1880L MM770G BLE MG

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·January 11, 2024

PUMP 1886 780G OUS BLE PUMP MG/DL

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·June 15, 2023

COCHLEAR OSIA OSI200 IMPLANT

FDA Adverse Event
Injury ·COCHLEAR LIMITED·Product code MCM·August 22, 2023

PROXIMATE*PPH PROCEDURE SET

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·April 24, 2019

630G INSULIN PUMP MMT-1715KL 630G

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·August 10, 2023

MINIMED 770G US SYSTEM BLE CONNECT 3.0 MG/DL

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·June 14, 2023

CAPSOCAM SV-3

FDA Adverse Event
Death ·CAPSOVISION, INC·Product code NEZ·July 11, 2024