57 results · 21ms · Sources: EU EUDAMED, US FDA

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Single Use Cytology Brush BC-205D

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

Marina Medical

FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306822308·Killian Nasal Speculum, Full Internal Groove, 3...

Hayden Medical

FDA UDI
Hayden Medical, Inc.·00840319721278·Buck Ear Curette 6-1/2" (16.3cm), size 2, blunt...

Easy Ambulatory

FDA UDI
CADWELL INDUSTRIES, INC.·00840067100585·Q-Video Mobile 2

OPTICHAMBER DIAMOND VALVED HOLDING CHAMBER

FDA 510(k)
FDA Class 2 ·Anesthesiology

ADVIA CENTAUR CALIBRATOR 30, MODELS 10379811/10379810

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

REZUM

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·October 6, 2025

REZUM

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·October 6, 2025

REZUM

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 18, 2025

ADVANCE 18 LP LOW PROFILE BALLOON CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code LIT·August 24, 2017

ADVANCE 18 LP LOW PROFILE BALLOON CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code LIT·August 24, 2017

REZUM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·March 13, 2026

REZUM

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 18, 2025

REZUM

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 18, 2025

SPIDERFX EMBOLIC PROTECTION DEVICE

FDA Adverse Event
Injury ·EV3 INC.·Product code NTE·October 6, 2008

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

FDA Adverse Event
Injury ·MEDTRONIC MINIMED·Product code MDS·July 19, 2011

FOXCROSS PTA CATHETER

FDA Adverse Event
Malfunction ·AV-TEMECULA-CT·Product code LIT·June 26, 2013

REZUM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·January 13, 2026

ADVANCE 18 LP LOW PROFILE BALLOON CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code LIT·May 31, 2017

ADVANCE 18 LP LOW PROFILE BALLOON CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code LIT·March 30, 2017