3,727 results
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31ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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 SÃ RL·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