5,060 results
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34ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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FDA UDI
SOUTHERN IMPLANTS (PTY) LTD·06009544011118·Instrument, Extension for Fixture Mount Hex, Long
NA
FDA UDI
SOUTHERN IMPLANTS (PTY) LTD·06009544011132·Instrument, Extension for Fixture Mount Hex, Short
NA
FDA UDI
SOUTHERN IMPLANTS (PTY) LTD·06009544011125·Instrument, Extension for Fixture Mount Hex, Me...
Softspan Tissue Expander
FDA UDI
Sientra, Inc.·00819409020324·Tissue Expander, Fleming & Mayer Design, Scalp,...
Softspan™ Tissue Expander
FDA UDI
SPECIALTY SURGICAL PRODUCTS INC·M746FMECX300S0·Softspan™ Scalp Tissue Expander, Fleming & Maye...
Softspan™ Tissue Expander
FDA UDI
SPECIALTY SURGICAL PRODUCTS INC·M746FMECV300S0·Softspan™ Scalp Tissue Expander, Fleming & Maye...
Softspan Tissue Expander
FDA UDI
Sientra, Inc.·00819409020317·Tissue Expander, Fleming & Mayer Design, Scalp,...
PALINDROME
FDA Adverse Event
Injury
·COVIDIEN MFG SOLUTIONS S.A.·Product code MSD·June 20, 2018
BD VACUTAINER® K2 EDTA (K2E) 5.4MG BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·August 7, 2023
HOW ROT HNG KNEE FME XL RGT
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS LIMERICK·Product code HSA·September 26, 2006
GOWN PLASTIC FILM IMPERVIOUS
FDA Adverse Event
Injury
·CARDINAL HEALTH·Product code FME·March 26, 2012
BD
FDA Adverse Event
Other
·BD & CO.·Product code FME·November 7, 2000
SYRINGE, EPIDURAL
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FME·January 15, 2001
PREVENTION PLUS CHEMO ISOLATION GOWN
FDA Adverse Event
Other
·MEDLINE INDUSTRIES, INC.·Product code FME·November 30, 2011
MEDLINE
FDA Adverse Event
Death
·MEDLINE INDUSTRIES, INC.·Product code FME·September 10, 2016
PATIENTSTYLE INFANT GOWN
FDA Adverse Event
Malfunction
·PATIENTSTYLE MEDICAL LLC·Product code FME·March 29, 2021
DERMATHERAPY
FDA Adverse Event
Injury
·Product code FME·April 12, 2018
RADSTIC RADIOLOGY MICROINTRODUCER KIT PTFE PEEL-APART SHEATH INTRO 4.5F X 10CM
FDA Adverse Event
Injury
·C.R. BARD, INC. (BASD) -3006260740·Product code DYB·April 15, 2022
LUCIRA CHECK-IT COVID-19 TEST
FDA Adverse Event
Malfunction
·PFIZER, INC·Product code QJR·June 5, 2024
AORTIC PERFUSION CANNULAE
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES·Product code DWF·November 8, 2019