25 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MEDTRONIC MINIMED PARADIGM INSULIN PUMPS
FDA 510(k)
FDA Class 2
·General Hospital
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756612364·Wrist Splint
JOBST soSoft
FDA UDI
BSN MEDICAL, INC.·00035664008093·SOSOFT 15-20 MM HG KNEE HIGH BROCADE MEDIUM BLA...
DURAVENT
FDA UDI
Andreas Fahl Medizintechnik-Vertrieb GmbH·04051948006841·DURAVENT XL 2 IC, SIZE 6
LOCATOR R-Tx
FDA UDI
Zest Anchors, LLC·00840481115875·Attachment System, 5.0mm/5.5mm/6.5mm Internal T...
LOCATOR F-Tx
FDA UDI
Zest Anchors, LLC·00840481123085·LOCATOR F-Tx Abutment for 5.0mm PrimaConnex Int...
General Instrument
FDA UDI
ALPHATEC SPINE, INC.·00840180513583·ALIF, Short Modular Rasped Rotating Distractor,...
Hayden Medical
FDA UDI
Hayden Medical, Inc.·00840319739822·Heaney Tissue Forceps 5-1/2" (13.8cm), 2x3 teeth
KermaX-plus
FDA UDI
IBA Dosimetry GmbH·EIBA1202060·KermaX Product family is designed to be install...
GUTTA PERCHA POINTS
FDA UDI
DiaDent Group International·08806383505499·Gutta Percha Points is used to root canal filin...
ELI 10 ELECTROCARDIOGRAPH MODEL ELI 10
FDA 510(k)
FDA Class 2
·Cardiovascular
INTRAORAL CAMERA ME-15
FDA 510(k)
FDA Class 1
·Dental
CHESAPEAKE® Stabilization System
FDA UDI
VB Spine LLC·10888857293977·3-Screw Drill Guide Inserter Size 10 mm
KermaX-plus
FDA UDI
IBA Dosimetry GmbH·EIBA120206S0·KermaX Product family is designed to be install...
Vu cPOD™
FDA UDI
Seaspine Orthopedics Corporation·10889981039219·Implant Non-Tapered 10x12x6mm (Non-Strut)
UNKNOWN PRODUCT - SET SCREW
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS KIEL·Product code HWC·October 12, 2012
ASR XL TAP SLV ADAP 12/14+2
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·May 20, 2013
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE CORPORATION·Product code KDJ·September 25, 2014
CARDIOVASCULAR PROCEDURE KIT
FDA Adverse Event
Injury
·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code OEZ·June 6, 2011
ENDURANT ILIAC STENT GRAFT
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code MIH·November 26, 2024