3,727 results · 31ms · Sources: EU EUDAMED, US FDA

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HDP

FDA UDI
Quality Aspirators, Inc.·00814005023120·HDP

OVATION HDP

FDA 510(k)
FDA Class 1 ·Ear, Nose, Throat

HDP-02

FDA UDI
Quality Aspirators, Inc.·00814005024349·HDP-02

HADRON FPLS INFINITY, HDP

FDA UDI
Infinitus Medical Technologies LLC·00860003986882·

ZERO PHACO HDP 2.2MM 30D 12B

FDA UDI
Bausch & Lomb GmbH·04058935000622·Single Use Medical Device for Ophthalmic Surgery

ZERO PHACO HDP 30DEG 12/B

FDA UDI
Bausch & Lomb GmbH·04058935000615·Single Use Medical Device for Ophthalmic Surgery

QUICKIE REVOLUTION WHEELCHAIR

FDA Adverse Event
Malfunction ·SUNRISE MEDICAL HDP·Product code IOR·August 10, 1999

MICS SIL I/A HDP 45° STELL 12B

FDA UDI
Bausch & Lomb GmbH·04058935000516·Single Use Medical Device for Ophthalmic Surgery

X3 TRIATHLON CS INSERT #2 13MM

FDA Adverse Event
Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·June 12, 2019

TRIATHLON CS INS SIZE 6 11MM

FDA Adverse Event
Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·January 1, 2020

I/A HDP. 45 W SLEEVE 1.8 12/BX

FDA UDI
Bausch & Lomb GmbH·04058935000202·Single Use Medical Device for Ophthalmic Surgery

MICS SIL I/A HDP 45° STELL 1/B

FDA UDI
Bausch & Lomb GmbH·04058935000523·Single Use Medical Device for Ophthalmic Surgery

UNSPECIFIED PLUM 360 PUMP

FDA Adverse Event
Malfunction ·ICU MEDICAL COSTA RICA LTD.·Product code FRN·March 28, 2023

VITAL SIGNS¿ HEAD POSITIONER

FDA Adverse Event
Malfunction ·Product code CCX·September 24, 2021

VITAL SIGNS¿ HEAD POSITIONER

FDA Adverse Event
Malfunction ·Product code CCX·September 24, 2021

INFINITY¿ TOTAL ANKLE SYSTEM

FDA Adverse Event
Injury ·WRIGHT MEDICAL TECHNOLOGY INC·Product code HSN·June 28, 2022

RGDLOOP ADJUSTABLE STND

FDA Adverse Event
Malfunction ·MEDOS INTERNATIONAL SàRL·Product code MBI·May 2, 2024

VITAL SIGNS¿ HEAD POSITIONER

FDA Adverse Event
Injury ·VYAIRE MEDICAL·Product code CCX·June 25, 2022

VITAL SIGNS¿ HEAD POSITIONER

FDA Adverse Event
Injury ·VYAIRE MEDICAL·Product code CCX·June 25, 2022

VAPR S90 4.0MM W/INTEGR HDP -EA

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code GEI·October 20, 2021