58 results · 23ms · Sources: EU EUDAMED, US FDA

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Kalitec Universal Instruments

FDA UDI
Kalitec Direct LLC·B07301K1102250·Tray, Base, 2.25", Universal

ANGIODYNAMICS, INC. VENACURE 1470 LASER

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

PRINCETON

FDA UDI
Princeton Medical Group, Inc.·00810158214712·PROBE BUTTONED WITH EYE 2MMØ 10"

DeRoyal

FDA UDI
DEROYAL INDUSTRIES, INC.·00749756814157·RIGID COLLAR

ELMED

FDA UDI
ELMED INCORPORATED·00198506058592·Tissue Forceps 10" w/o Teeth Serr

PRINCETON

FDA UDI
Princeton Medical Group, Inc.·00810158212886·FORCEPS STANDARD DRESSING STRAIGHT 10"

SAV

FDA UDI
Diversified Products, Inc.·00842894116944·

Arthrex®

FDA UDI
ARTHREX, INC.·00888867500723·Full Ring, 225mm

DOSIMETRY CHECK

FDA 510(k)
FDA Class 2 ·Radiology

PULSE OXIMETER MODEL P10

FDA 510(k)
FDA Class 2 ·Cardiovascular

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·June 7, 2023

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·October 23, 2023

LOGIC TIBIA IMPLANT PSC INSERT, SZ 2.5, 13MM

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·February 28, 2023

TRULIANT TIB IMP PS INSERT SZ 2.5 11MM

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·April 14, 2023

RESERVOIR 3ML

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·May 13, 2013

E SERIES DEFIBRILLATOR

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·May 20, 2011

ACCU-CHEK COMFORT CURVE TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·August 14, 2008

ADVANCED PATELLA 29M 3 PEG IMPLANT

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·October 8, 2024

FOSTEOSELECT DBM PUTTY

FDA Adverse Event
Injury ·BACTERIN·Product code MQV·November 29, 2012

TRULIANT TIB IMP PS INSERT SZ 2.5 10MM

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·July 16, 2024