8,753 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HNR-PC HIP
FDA 510(k)
FDA Class 2
·Orthopedic
HOWMEDICA HNR SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
V. Mueller
FDA UDI
STERIS CORPORATION·10885403431234·V. Mueller MODULAR HANDLE NON-RATCHETED
HOWMEDICA(R) HNR SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
77-301605 20"HIGH PRESSURE LINE W/RA
FDA Adverse Event
Malfunction
·DEROYAL·Product code LRP·April 23, 2001
HOWMEDICA HARRIS HIP AND CUP
FDA Adverse Event
Malfunction
·HOWMEDICA, INC.·Product code KWB·August 1, 1994
HNR PR1 STEM 135X43MM SM
FDA Adverse Event
Malfunction
·HOWMEDICA INC.·Product code KWY·May 21, 1997
HNR PR1 STEM 135X33MM SM
FDA Adverse Event
Malfunction
·HOWMEDICA INC.·Product code KWY·April 29, 1998
UNKNOWN_COCR FEMORAL HEAD
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·July 20, 2020
UNKNOWN_STRYKER STEM
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·July 20, 2020
ON-Q C-BLOC 400ML, 2-14ML; HR SELECT-A-FLOW
FDA Adverse Event
Malfunction
·HALYARD·Product code MEB·April 10, 2015
Brand Name: MST Duet Reusable Handle for Single Use Heads Product Name: Reusable Handle for Single Use Heads (Forceps and Scissors) Model/Catalog Number: DFH-1028 Software Version: N/A Product Description: A MST Single Use Forceps or Scissors System consists of a reusable handle and one of a number of single use interchangeable heads. MST Single Use Forceps and Scissor heads are shipped ready to use sterile in a tray with Tyvek lid within a sterile pouch. MST Duet Reusable Handle for Single Use Forceps & Scissor Heads are supplied in a non-sterile condition and must be sterilized prior to and after every use. The blue sleeve the handle is packaged in is not intended to be sterilized and does not maintain sterility. Component: Yes. The MST Duet¿ Reusable Handle for Single Use Heads is the reusable handle component which connect to either Single Use Forceps or Scissors heads.
FDA Enforcement
Class II
·Ongoing·MicroSurgical Technology Inc·December 4, 2024
GRIESHABER REVOLUTION DSP FORCEPS
FDA Adverse Event
Malfunction
·ALCON GRIESHABER AG·Product code HNR·October 17, 2016
MINI DIAMOND FORCEPS TIP, 1.3MM
FDA Adverse Event
Malfunction
·ALCON GRIESHABER AG·Product code HNR·February 20, 2009
MST SIEBEL CAPSULORHEXIS FORCEPS
FDA Adverse Event
Malfunction
·MICROSURGICAL TECHNOLOGY, INC.·Product code HNR·April 11, 2014
REVOLUTION DSP 25G FORCEPS
FDA Adverse Event
Malfunction
·ALCON GRIESHABER AG·Product code HNR·March 12, 2010
REVOLUTION DSP 23G, ILM FORCEPS
FDA Adverse Event
Malfunction
·ALCON GRIESHABER AG·Product code HNR·May 27, 2010
STORZ O'BRIEN FIXATION FORCEPS
FDA Adverse Event
Malfunction
·STORZ INSTRUMENT COMPANY·Product code HNR·September 27, 1996
CHANG IOL FORCEPS
FDA Adverse Event
SYNERGETICS, INC.·Product code HNR·July 2, 1996
FORCEPS
FDA Adverse Event
Malfunction
·ALCON LABORATORIES, INC.·Product code HNR·February 6, 2004