12 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
UNIPOWER RECHARGEABLE BATTERY PACK
FDA 510(k)
FDA Class 1
·Anesthesiology
SYNELISA SM ABS/RNP-SM ABS
FDA 510(k)
FDA Class 2
·Immunology
BIOTROL AMYLASE CNPG3
FDA 510(k)
FDA Class 2
·Clinical Chemistry
FEMORAL HEAD STERILE PRODUCT
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code LPH·November 24, 2021
UNSPECIFIED SAFESET TRANSPAC SETS
FDA Adverse Event
Malfunction
·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code DRS·January 2, 2025
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·January 30, 2013
ENDOPATH** XCEL*
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·December 22, 2010
ANIMAS INSULIN CARTRIDGE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 15, 2014
WAGNER CONE PROSTHESIS, 135, UNCEMENTED¸ 14, TAPER 12/14
FDA Adverse Event
Malfunction
·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code LZO·November 26, 2021
LINER 10 DEGREE ELEVATED RIM 22
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·November 24, 2021
FEMORAL STEM PRESS-FIT COLLARLESS 12/14
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·December 14, 2021
MODIFIED KUGEL PATCH
FDA Adverse Event
Injury
·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·May 25, 2016