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

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RUBBERCARE GUARDIAN POLYMER-COATED POWDER-FREE LATEX EXAMINATION GLOVES: CONTAINS 100 MICROGRAMS OR LESS OF TOTAL WATER

FDA 510(k)
FDA Class 1 ·General Hospital

Sterling C2000

FDA UDI
SKYTRON LLC·10841736123215·C2000 Standard Rack for Containers

CTXA Hip Bone Mineral Densitometer

FDA UDI
MINDWAYS SOFTWARE, INC.·B052DICTXAHIP0·The CTXA Hip Bone Mineral Densitometer (CTXA Hi...

ADVANCE®

FDA UDI
Microport Orthopedics Inc.·M684K00271141·

artVeneer life

FDA UDI
Merz Dental GmbH·D7092002114·artVeneer life upper posteriors, M, C3

BetaForce

FDA UDI
ORTHO TECHNOLOGY, INC.·00190730022035·Beta3 Euro Upper 018 10 archwires per pack

BetaForce™

FDA UDI
Ortho Organizers, Inc.·00190707124441·BETAFORCE Beta³ Euro Upper .018 (10pk)

SCANLAN®

FDA UDI
SCANLAN INTERNATIONAL INC·00846159018103·Dennis Peripheral Vascular Clamp

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112830·BARRON VACUUM PUNCH 9.5MM

3M QUIK TEMP TEMPORIZATION MATERIAL

FDA 510(k)
FDA Class 2 ·Dental

RS-4M+MUSCLE STIMULATOR

FDA 510(k)
FDA Class 2 ·Physical Medicine

HEYER-SCHULTE BREAST IMPLANT, 150 CC

FDA Adverse Event
V. MUELLER DIV. BAXTER HEALTHCARE CORP.·Product code FTR·May 19, 1994

HEYER-SCHULTE BREAST IMPLANT, 165 CC

FDA Adverse Event
V. MUELLER DIV. BAXTER HEALTHCARE CORP.·Product code FTR·May 19, 1994

3008261720-2024-002114

FDA Adverse Event
Injury ·JJGC INDUSTRIA E COMERCIO DE MATERIAIS DENTARIOS SA·Product code DZE·August 8, 2024

AUTOSOFT XC

FDA Adverse Event
Injury ·UNOMEDICAL UM-D·Product code FPA·January 13, 2025

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·September 14, 2011

TRANS-RAY PLUS 7.5FR 40CC IAB WITH ACCESSORIES

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·April 3, 2024

HEARTSINE SAMARITAN 300P AND PAD PAK

FDA Adverse Event
Malfunction ·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·February 11, 2013

HIRES 90K

FDA Adverse Event
Malfunction ·ADVANCED BIONICS LLC·Product code MCM·January 31, 2011

ACCU-CHEK AVIVA TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·February 20, 2008