36 results
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29ms
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Sources: EU EUDAMED, US FDA
STRYKER (R) PATIENT SPECIFIC POLYMER IMPLANT
FDA 510(k)
FDA Class 2
·Neurology
GUEDEL AIRWAY, SIZE 1, ISO 6.5
FDA UDI
Intersurgical Incorporated·05030267050611·GUEDEL AIRWAY, SIZE 1, ISO 6.5
Batrik Non-Sterile Suture Tags Blue 5
FDA UDI
Batrik Medical Manufacturing Inc·00690521011076·"Suture Clamp Tags, Radio Opaque, Non-Sterile, ...
Batrik Suture Tags Blue 5 pairs
FDA UDI
Batrik Medical Manufacturing Inc·00690521014398·"Suture Clamp Tags, Radio Opaque, Sterile, Blue...
MicroSelectron Digital
FDA UDI
Nucletron B.V.·08717213015487·microSelectron Transfer Tube for 5F Flexibles (13)
Surgical Instrument
FDA UDI
Jeil Medical Corporation·08809282815607·
SI-RESTORE
FDA UDI
BIOFUSION MANAGEMENT AND MANUFACTURING, LLC·00850073363133·SI-RESTORE SCREW, 11.0MM x 65MM
SI-RESTORE
FDA UDI
BIOFUSION MANAGEMENT AND MANUFACTURING, LLC·00850073363614·SI-RESTORE SCREW, HA BLASTED, 11.0MM x 65MM
Ø11mm Sacroiliac Falco Fusion Screw - L65mm
FDA UDI
McNicoll Chirurgical Inc.·07540161800079·Ø11mm Sacroiliac Falco Fusion Screw - L65mm
Summa Orthopaedics System Surgical Instrument
FDA UDI
Jeil Medical Corporation·08806390864046·
Portex
FDA UDI
ICU MEDICAL, INC.·15019315018923·
Surgical Instrument
FDA UDI
Jeil Medical Corporation·08809282815614·
VersiTomic Low Profile Ø6.5 mm
FDA UDI
T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION·10818674028377·
SPAULDING IQ ELECTROCARDIOGRAPH
FDA 510(k)
FDA Class 2
·Cardiovascular
INTRACORPOREAL ULTRASOUND LITHOTRIPTER, MODEL 2271.004, ULTRASOUND TRANSDUCER, MODEL 2271.501, ULTRASOUND PROBES (SONO)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Summa Orthopaedics System Surgical Instrument
FDA UDI
Jeil Medical Corporation·08806390864053·
MAXCEM ELITE CLEAR
FDA Adverse Event
Malfunction
·KERR CORPORATION·Product code EMA·May 14, 2013
SUPER POLIGRIP FREE DENTURE ADHESIVE CREAM
FDA Adverse Event
Other
·GLAXOSMITHKLINE·Product code KOL·May 23, 2011
ENDOPATH ILS ENDOSCOPIC CURVED INTRALUMINAL STAPLER - 29MM
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, LLC.·Product code KOG·August 13, 2008
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·May 7, 2022