13 results · 19ms · Sources: EU EUDAMED, US FDA

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SUTURE REMOVAL SET CAT.#906

FDA 510(k)
FDA Class 1 ·General, Plastic Surgery

Polishers

FDA UDI
DFS - DIAMON GmbH·04057176161147·UPORAL D cup small, pu: 2 pcs

Symmetry Surgical

FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482032299·Symmetry® Forceps, Symmetry Tying, Curved, 7 in

RETROGRADE CARDIOPLEGIA CANNULA, SELF-INFLATING, WITH MALLEABLE OR GUIDEWIRE STYLET

FDA 510(k)
FDA Class 2 ·Cardiovascular

FREEDOM TOTAL KNEE SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

FLOSEAL

FDA Adverse Event
Injury ·BAXTER HEALTHCARE CORPORATION·Product code LMF·January 3, 2020

FLOSEAL

FDA Adverse Event
Injury ·BAXTER HEALTHCARE CORPORATION·Product code LMF·January 3, 2020

MENTOR SILTEX ROUND MODERATE PROFILE

FDA Adverse Event
Injury ·MENTOR TEXAS·Product code FWM·June 4, 2019

ABL800 FLEX

FDA Adverse Event
Malfunction ·RADIOMETER MEDICAL APS·Product code CHL·February 12, 2014

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

FDA Adverse Event
Injury ·MEDTRONIC MINIMED·Product code OYC·October 23, 2012

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN, INC.·Product code NBW·August 16, 2010

DORO¿ Easy-Connect Navigation Adaptor; BRAINLAB (item No. 1204.002)

FDA Enforcement
Class II ·Ongoing·Pro-Med Instruments Gmbh·June 4, 2025

Product Label - ACUSON Sequoia *** Power Input: 100-240V~, 13.0-5.4A, 50-60Hz *** (240)11148775 Model User Manual states - ACUSON Sequoia Diagnostic Ultrasound Systems

FDA Enforcement
Class II ·Ongoing·Siemens Medical Solutions USA, Inc.·April 7, 2021