24 results · 24ms · Sources: EU EUDAMED, US FDA

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VICTUS Femtosecond Laser Platform

FDA 510(k)
FDA Class 2 ·Ophthalmic

Mueller Blister Kit

FDA UDI
Mueller Sports Medicine, Inc.·00074676207247·BLISTER KIT

OsteoMed

FDA UDI
OSTEOMED LLC·00845694017862·MFx™ Lag Screw Cannula

BSSO/LFI INTERDNTL OSTETOMY 6mm

FDA UDI
W.H. Holden, Inc.·D9282007240·

Deltec

FDA UDI
ICU MEDICAL, INC.·00610586024019·

BSSO/LFI INTERDNTL OSTY 8mm

FDA UDI
W.H. Holden, Inc.·D92820072410·

MEDICA HP 300 HEMOFILTRATION PUMP, MODEL 300

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

DIMENSION AUTOMATED LDL CHOLESTEROL FLEX REAGENTCARTRIDGE METHOD, MODEL DF131

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

AUVON TENS & EMS DEVICE

FDA Adverse Event
Injury ·SHEN ZHEN AS TEC TECHNOLOGY CO LTD·Product code NUH·January 28, 2025

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·July 29, 2025

DEXCOM G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM, DEXCOM SHARE SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code MDS·December 10, 2015

VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAM·July 20, 2019

VITROS 5,1 FS CHEMISTRY SYSTEM

FDA Adverse Event
Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code JJE·August 11, 2011

DEPUY ASR XL FEM IMP SIZE 49

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·October 24, 2014

OBTRYX SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·July 1, 2013

GORE VIABAHN ENDOPROSTHESIS

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES,INC·Product code NIP·October 29, 2007

AUVON TENS UNIT

FDA Adverse Event
Injury ·SHEN ZHEN AS TEC TECHNOLOGY CO LTD·Product code NUH·December 19, 2024

UNKNOWN CAGE/SPACER

FDA Adverse Event
Injury ·MEDOS INTERNATIONAL SàRL CH·Product code OVD·June 2, 2021

UNKNOWN CAGE/SPACER

FDA Adverse Event
Injury ·MEDOS INTERNATIONAL SàRL CH·Product code OVD·June 2, 2021

PROXIMATE*HCS HEMORR CIR STAPL (EXACT CODE UNKNOWN

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 20, 2019