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

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BD PROBETEC CHLAMYDIA TRACHOMATIS (CT) QX AMPLIFIED DNA ASSAY

FDA 510(k)
FDA Class 1 ·Microbiology

Orthopedic manual surgical instrument

FDA UDI
BAUI BIOTECH CO. LTD.·04715862873575·Poly Axial Screw Driver

LEONE SPA

FDA UDI
LEONE SPA·08033707065708·INTRAORAL ELASTICS 4,5 oz 1/4" red

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450047903·

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197513548·RZ Tebbet Breast Retractor 90x24m...

PERSONAL INFUSOR LOCAL PAIN MANAGEMENT PROCEDURAL KIT

FDA 510(k)
FDA Class 2 ·General Hospital

PERCUTANEOUS INTRODUCER, MODEL 10383-XXX

FDA 510(k)
FDA Class 2 ·Cardiovascular

TGS UKA SYSTEM

FDA Adverse Event
Injury ·ALEXANDRIA RESEARCH TECHNOLOGIES, INC·Product code HSX·March 22, 2013

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·April 17, 2025

TGS UKA KNEE SYSTEM

FDA Adverse Event
Injury ·ALEXANDRIA RESEARCH TECHNOLOGIES, INC.·Product code HSX·May 6, 2013

ADULT DUAL HEATED BREATHING CIRCUIT

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE, LTD.·Product code BZE·December 8, 2009

TGS UKA SYSTEM

FDA Adverse Event
Injury ·CAYENNE MEDICAL, INC·Product code HSX·February 12, 2014

TGS UKA SYSTEM

FDA Adverse Event
Injury ·CAYENNE MEDICAL, INC.·Product code HSX·September 25, 2014

UNKNOWN GEL IMPLANTS

FDA Adverse Event
Injury ·MENTOR TEXAS·Product code FTR·December 27, 2019

UNKNOWN GEL IMPLANTS

FDA Adverse Event
Injury ·MENTOR TEXAS·Product code FTR·December 27, 2019

TGS UKA SYSTEM

FDA Adverse Event
Injury ·CAYENNE MEDICAL INC.·Product code HSX·May 15, 2014

TGS UKA KNEE SYSTEM

FDA Adverse Event
Injury ·ALEXANDRIA RESEARCH TECHNOLOGIES, INC.·Product code HSX·September 10, 2013

TGS UKA KNEE SYSTEM

FDA Adverse Event
Injury ·ALEXANDRIA RESEARCH TECHNOLOGIES, LLC·Product code HSX·August 14, 2013

XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM

FDA Adverse Event
Malfunction ·AV-TEMECULA-CT·Product code NIQ·May 2, 2013

TERUMO ADVANCED PERFUSION SYSTEM 1

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·April 26, 2011