1,033 results
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35ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ETHI-PAK
FDA UDI
Ethicon Inc.·10705031036727·Stainless Steel, Nonabsorbable Surgical Suture
CC25 Ion chamber
FDA UDI
IBA Dosimetry GmbH·EIBADS221000·CC25 Ion chamber: 0.25 ccm, shonka plastic, w...
CC25 Ion chamber
FDA UDI
IBA Dosimetry GmbH·EIBADS220000·CC25 Ion chamber: 0.25 ccm, shonka plastic, w...
Bariatric Heavy Duty Wheelchair (YJ-010B 20DS; YJ-010B 20DE; YJ-010B 20DFS; YJ-010B 20DFE;YJ-010B 20ADS; YJ-010B 20ADE; YJ-010B 20ADFS; YJ-010B 20ADFE; YJ-010B 22DS; YJ-010B 22DE; YJ-010B 22DFS;YJ-010B 22DFE; YJ-010B 22ADS;YJ-010B 22ADE; YJ-010B 22ADFS; YJ-010B 22ADFE; YJ-010B 24DS; YJ-010B 24DE; YJ-010B 24DFS; YJ-010B 24DFE; YJ-010B 24ADS; YJ-010B 24ADE; YJ-010B 22ADFS; YJ-010B 24ADFE)
FDA 510(k)
FDA Class 1
·Physical Medicine
EVIS LUCERA ELITE BRONCHOVIDEOSCOPE
FDA Adverse Event
Injury
·AIZU OLYMPUS CO., LTD.·Product code EOQ·July 25, 2023
THORATEC® HEARTMATE 3® LVAS IMPLANT KIT
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·January 9, 2025
PREMILENE/MONOSYN SET
FDA Adverse Event
Malfunction
·B.BRAUN SURGICAL S.A.·Product code GAW·August 7, 2015
INOMAX DS (DELIVERY SYSTEM)
FDA Adverse Event
Injury
·INO THERAPEUTICS LLC.IKARIA·Product code MRN·November 16, 2011
INOMAX DE (DELIVERY SYSTEM)
FDA Adverse Event
Malfunction
·INO THERAPEUTICS LLC / IKARIA·Product code MRN·July 30, 2010
PINN MAR NEUT 28IDX46OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 21, 2020
SPYSCOPE DS II ACCESS & DELIVERY CATHETER
FDA Adverse Event
Death
·BOSTON SCIENTIFIC CORPORATION·Product code FBN·December 22, 2025
KENEX
FDA UDI
KENEX (ELECTRO-MEDICAL) LIMITED·05055449405928·48cm curtain & collision tolerant pivotal arm
AMPLATZ SUPER STIFF
FDA Adverse Event
Death
·BOSTON SCIENTIFIC CORPORATION·Product code DQX·January 29, 2026
MICRA
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code PNJ·January 11, 2021
LUPINE BR DS W/ORTHCRD
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code MAI·April 1, 2024
FUKUDA DENSHI MODEL DS-5700 CENTRAL STATION
FDA Adverse Event
Malfunction
·FUKUDA DENSHI CO., LTD.·Product code DSI·December 15, 2004
NAVITOR VISION
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code NPT·June 27, 2025
CANDELA GENTLEMAX LASER SYSTEM
FDA Adverse Event
Malfunction
·CANDELA CORPORATION·Product code GEX·April 7, 2017
NAVITOR TRANSCATHETER AORTIC VALVE
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code NPT·April 16, 2026
FLEXNAV DELIVERY SYSTEM
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code NPT·October 31, 2025