7,375 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Pulse by EHE Health
FDA UDI
WELLDOC, INC.·B553PULSE100·Pulse by EHE Health (“Pulse”) is a Software as ...
Pulse Rx by EHE Health
FDA UDI
WELLDOC, INC.·B553PULSERX100·Pulse Rx by EHE Health (“Pulse”) is a Software ...
COLLEAGUE VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·March 15, 2005
PRECISION SPECTRA
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 1, 2021
ENDOPATH ETS45 ENDOSCOPIC LINEAR CUTTER - 2.5 MM
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code KOG·June 3, 2004
PALMAZ-SCHATZ BALLOON EXPANDABLE STENT WITH DELIVERY SYSTEM
FDA Adverse Event
Injury
·*·Product code MAF·February 26, 1997
TRIDENT 10° CROSSFIRE INSERT 36 MM ID
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·August 15, 2014
D-TRONPLUS
FDA Adverse Event
Malfunction
·DISETRONIC MEDICAL SYSTEMS, INC.·Product code LZG·October 13, 2006
HALLU-S PLATE SIZE 1 LEFT
FDA Adverse Event
Other
·NEWDEAL·Product code HRS·July 19, 2010
SERACLONE ANTI-E (RH5)
FDA Adverse Event
Malfunction
·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code KSF·May 20, 2011
VEST
FDA Adverse Event
Injury
·HILL-ROM CHARLESTON·Product code BYI·January 4, 2006
TYTIN FC
FDA Adverse Event
Malfunction
·KERR CORP. KERR USA·Product code EHE·August 27, 1999
IMPLANTABLE COLLAMER LENS (ICL)
FDA Adverse Event
Injury
·STAAR SURGICAL COMPANY·Product code QCB·February 7, 2024
PUMP 381 PUMP SET (US)
FDA Adverse Event
Death
·ABIOMED, INC. - 1220648·Product code OZD·February 6, 2026
IMPELLA
FDA Adverse Event
Injury
·ABIOMED, INC. - 1220648·Product code OZD·February 6, 2026
OPTICAL, AIC, IMPELLA CONNECT, PKGD, US
FDA Adverse Event
Death
·ABIOMED, INC. - 1220648·Product code OZD·January 15, 2026
PUMP 371 14F LT CMR SET
FDA Adverse Event
Injury
·ABIOMED, INC. - 1220648·Product code OZD·February 12, 2026
LIBERTY CYCLER SET, SINGLE CONN./EXT. DL
FDA Adverse Event
Injury
·ERIKA DE REYNOSA, S.A. DE C.V.·Product code FKX·August 24, 2017
Dispenser, Mercury And/Or Alloy
FDA classification
FDA Class 1
·Dispenser, Mercury And/Or Alloy
KERECIS EHF
FDA registration
KERECIS EHF·4 products·🇮🇸 Iceland