28 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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4635 ASSISTANT'S INSTRUMENTATION
FDA 510(k)
FDA Class 1
·Dental
PowerPICC Provena SOLO
FDA UDI
Bard Access Systems, Inc.·00801741202063·Catheter Placement Kit
Preat
FDA UDI
Preat Corporation·00842092165867·NobelActive™/Conical-compatible RP Titanium Bla...
AtriClip® LAA Exclusion System
FDA UDI
ATRICURE, INC.·00818354015058·AtriClip® PRO2 Gillinov-Cosgrove LAA Exclusion ...
Epredia
FDA UDI
RICHARD-ALLAN SCIENTIFIC COMPANY·00673693214360·Cassettes are designed to contain incised tissu...
AtriClip® PRO2 Gillinov-Cosgrove LAA Exclusion System
FDA UDI
ATRICURE, INC.·10840143912085·LAA Exclusion System, PRO245
AtriClip® LAA Exclusion System
FDA UDI
ATRICURE, INC.·10840143900198·AtriClip® PRO2 Gillinov-Cosgrove LAA Exclusion ...
AtriClip® LAA Exclusion System
FDA UDI
ATRICURE, INC.·10840143907418·AtriClip® PRO2 Gillinov-Cosgrove LAA Exclusion ...
Preat Implant Prosthetics
FDA UDI
Preat Corporation·00842092165874·NobelActive™/Conical-compatible RP – Milled Ti...
REF SHADE
FDA UDI
AMERICAN TOOTH INDUSTRIES·D772ATI250009670·3-OZ REF SH-67 TOOTH SHADE COLD CU
SECURMIX
FDA 510(k)
FDA Class 2
·General Hospital
ALKALINE PHOSPHATASE LIQUID REAGENT-KINETIC, MODELS A504-150 AND A504-500H
FDA 510(k)
FDA Class 2
·Clinical Chemistry
ANESTAR
FDA Adverse Event
Malfunction
·MINDRAY DS USA, INC.·Product code BSZ·March 30, 2009
6800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 27, 2013
PRECISION
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·February 18, 2011
CONTEGRA PULMONARY VALVED CONDUIT
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES, INC.·Product code MWH·February 15, 2008
Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967
FDA Recall
Open, Classified
·Preat Corp·Product code NHA·February 9, 2024
BD TRUCOUNT TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·July 13, 2021
Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967
FDA Enforcement
Class II
·Ongoing·Preat Corp·March 27, 2024
BD TRUCOUNT TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON CARIBE LTD.·Product code GKZ·July 15, 2021