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

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Force TriVerse Electrosugical Device, Holster, 10-foot, Force TriVerse Electrosurgical Device, Holster, 15-foot

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

HHM

FDA UDI
Oticon A/S·05707131281128·H160V2, MINIBTE 312 WL 85 TC HHM

Ophthalmic Speculum

FDA UDI
KATENA PRODUCTS, INC.·00841668100202·NEVYAS DRAPE SPECULUM OPEN WIRE

Symmetry Surgical Ultra®

FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482049105·Ultra Instruments Clamp; Bulldog Vein Clamp; St...

MC6A

FDA 510(k)
FDA Class 2 ·Dental

POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)

FDA 510(k)
FDA Class 1 ·General Hospital

HNM MEDICAL

FDA UDI
HNM STAINLESS, LLC.·00842962111123·BULLDOG VEIN CLAMP, 1 1/4", CVD, TITANIUM

VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

FDA Adverse Event
Injury ·COOK VASCULAR INC·Product code LJT·January 7, 2016

XIENCE PRIME EVEROLIMUS ELUTING CORONARY STENT SYSTEM

FDA Adverse Event
Malfunction ·AV-TEMECULA-CT·Product code NIQ·June 6, 2013

HOMECHOICE AUTOMATED PD SET WITH CASSETTE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 6, 2011

GE OEC 9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 9, 2008

REVEAL XT

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code DSI·December 7, 2017

VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

FDA Adverse Event
Malfunction ·COOK VASCULAR INC·Product code LJT·January 3, 2019

VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

FDA Adverse Event
Malfunction ·COOK VASCULAR INC·Product code LJT·January 3, 2019

ROI-C IMPLANT, UNKNOWN SIZE

FDA Adverse Event
Injury ·LDR MÉDICAL·Product code OVE·September 21, 2021

VITAL-PORT

FDA Adverse Event
Injury ·COOK VASCULAR INC·Product code LJT·May 24, 2016