29 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HARDYDISK, CEFAZOLIN, 30MCG
FDA 510(k)
FDA Class 2
·Microbiology
Deployment Skid Cannula Access Tool
FDA UDI
Anika Therapeutics, Inc.·00817337000319·Reusable non-rigid cannula access tool
PowerPICC
FDA UDI
Bard Access Systems, Inc.·00801741042584·Catheter Placement Kit
ADVANCE®
FDA UDI
Microport Orthopedics Inc.·M684K00012881·
TruFlex™
FDA UDI
Ortho Organizers, Inc.·00190707127299·Truflex™ PT SE NiTi Upper 17x25 34mm (10PK)
TruFlex
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730011848·Truflex™ PT SE NiTi Upper 17x25 34mm 10/PK
CURE™ ACP
FDA UDI
MEDITECH SPINE, LLC·B167700001280·
CURE 2.0 ACP
FDA UDI
SpineArt SA·07640375232328·ANTERIOR CERVICAL PLATE, 1 LEVEL L28
CURE™ ACP
FDA UDI
MEDITECH SPINE, LLC·B167S1700001280·
CURE 2.0 ACP
FDA UDI
SpineArt SA·07640375230935·CERVICAL 1 LEVEL TEMPLATE L28
RENAFLO II HF 2000 HEMOFILTER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
RAPID RHINO-ANTERIOR 90MM, MODEL RR-A 90, RAPID RHINO-POSTERIOR 100MM, MODEL RR-P 100
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
SMR REVERSE HUMERAL BODY
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code KWS·October 21, 2022
NIROYAL BILIARY STENT
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION, IRELAND, LTD.·Product code FGE·July 31, 2002
ULTRA-THIN BALLOON DILATATION CATHETER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION, IRELAND, LTD.·Product code LIT·July 31, 2002
WALLACH ULTRA FREEZE
FDA Adverse Event
Malfunction
·COOPERSURGICAL, INC.·Product code GEH·July 11, 2023
LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM 9.75CM
FDA Adverse Event
Malfunction
·ALLERGAN·Product code LTI·February 14, 2013
POWER PRO AMBULANCE COT
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code INK·February 3, 2011
LUGE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC·Product code DQX·February 19, 2008
ADVANTA V12,COVERED STENTSYS,10X59X120
FDA Adverse Event
Malfunction
·ATRIUM MEDICAL CORPORATION·Product code NIO·December 10, 2025