14 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ATRAMAT
FDA UDI
Internacional Farmacéutica, S.A. de C.V.·07500142063756·ATRAMAT SILK SURGICAL SUTURE BLACK USP 3-0 EP 2...
TD-4140 Smart Dongle Blood Glucose plus B-ketone Monitoring System
FDA 510(k)
FDA Class 1
·Clinical Chemistry
PIVOX™ Oblique Lateral Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00763000878474·TRIAL 2173345 O25 IB 20MM 18 DEG 12X45
PIVOX™ Oblique Lateral Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169600010·TRIAL 2173345 O25 IB 20MM 18 DEG 12X45
ATRAMAT
FDA UDI
Internacional Farmacéutica, S.A. de C.V.·07500142068775·ATRAMAT SILK SURGICAL SUTURE BLACK USP 4-0 EP 1...
CERTAIN CONTOURED MARGIN CERAMIC ABUTMENT
FDA 510(k)
FDA Class 2
·Dental
BREATHE TECHNOLOGIES VENTILATOR AND ACCESSORIES (BT-V2S)
FDA 510(k)
FDA Class 2
·Anesthesiology
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·July 7, 2025
DISCOVERY RF180
FDA Adverse Event
Injury
·GENERAL MEDICAL MERATE S.P.A.·Product code JAA·August 2, 2023
BD NEXIVA¿ DIFFUSICS¿ CLOSED IV CATHETER SYSTEM
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·July 22, 2022
NEXIVA DIFFUSICS
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·March 30, 2026
3.0MM TI STERNAL LCKNG SCREW SELF-DRILLING/20MM
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HRS·June 17, 2013
LIGAMAX-5MM
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code FZP·July 23, 2011
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 10, 2014