7,375 results · 28ms · Sources: EU EUDAMED, 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