655 results
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22ms
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Sources: EU EUDAMED, US FDA
SEAC Advanced Dental System, Model A591561 The SEAC Advanced Dental System is a self-contained dental delivery system with a built-in air compressor,vacuum system and water supply. It is designed operate dental handpiece attachments and suction instruments. The SEAC Advanced Dental System can also be upgraded to include a Micadent air abrasion system mounted inside the unit with the handpiece mounted in a holder along side the other handpiece connections. The Micadent is used to perform intra oral air abrasion procedures including etching and preparing surfaces for composite restoration. The SEAC Advanced Dental System is substantially similar in design and functions as the SEAC Mobile Dental System manufactured by ASI Medical, Inc. The Micadent is manufactured by Medidents and will be supplied to ASIas a completed product. The Micadent is substantially the same as it is provided and is attached to an accessory air line inside the SEAC unit for operation. It is intended for use to provide general dental restorative care and hygiene procedures in both traditional dental office settings and/or mobile applications by or under the supervision of a licensed dentist or a hygienist if permitted by applicable law.
FDA Recall
Terminated
·ASI Medical, Inc.·Product code EIA·November 5, 2013
PRN 50-M+, GE part number 2062759-001, manufacturer part number 600-23310-01 Product Usage: The PRN 50M+ Paper Chart Recorder thermally records patient data on a paper strip. This device is intended for use under direct supervision of a licensed health care practitioner. This device is not intended for home use.
FDA Recall
Terminated
·Gsi Group Inc·Product code DSF·December 2, 2015
Dynex DSX Software-IVD ELISA Assays effected as follows: DSX Assay File Software: ZEUS vl B. burgdorferi lgG-lgM.asy ZEUS vl Borrelia VlsEl-pepClO lgG-lgM.asy ZEUS Parvovirus B19 lgG (9Z7701G).asy ZEUS Parvovirus B19 lgM (9Z7701M).asy ZEUS vl HSV-1 and 2 lgM.asy ZEUS vl Sm-RNP [CF] .asy ZEUS vl Sm-RNP [CV].asy ZEUS vl CMV lgG.asy ZEUS vl CMV lgM.asy ZEUS vl EBV-VCA lgG.asy ZEUS vl EBV-VCA lgM.asy ZEUS vl H. pylori lgG.asy ZEUS vl M. pneumoniae lgG.asy ZEUS vl M. pneumoniae lgM.asy ZEUS vl Measles lgG.asy ZEUS vl Mumps lgG .asy ZEUS vl T. gondii lgG .asy ZEUS vl T. gondii lgM.asy ZEUS vl VZV lgG.asy ZEUS vl Rubella lgG .asy ZEUS vl Rubella lgM.asy ZEUS vl MPO [CF].asy ZEUS vl MPO [CV].asy ZEUS vl EBNA-1 lgG.asy ZEUS vl.1 HSV-1 and 2 lgM.asy Product Usage: The DYNEX DSX Automated ELISA System is an open automated open system to perform ELISA immunoassay
FDA Recall
Terminated
·Zeus Scientific, Inc.·Product code N/A·July 22, 2019
Sterile Disposable Connectors ASY ASY STR CONN 3/8 STRLE 24 REF/ GTIN for Insert Label:050506000/ 00803622123238
FDA Recall
Terminated
·LivaNova USA Inc.·Product code DTL·April 24, 2020
Sterile Disposable Connectors ASY S CONN 3/16X1/8 RDR ANLD24 REF/ GTIN for Insert Label:050513000/ 00803622123252
FDA Recall
Terminated
·LivaNova USA Inc.·Product code DTL·April 24, 2020
Sterile Disposable Connectors ASY S/1/4 TO 3/16 RED 24 REF/ GTIN for Insert Label:050514000/00803622123269
FDA Recall
Terminated
·LivaNova USA Inc.·Product code DTL·April 24, 2020
FilmArray Blood Culture Identification (BCID) Panel Product Pouch Label: FilmArray BCID Panel Part No: RFIT-ASY-0126 Part No: RFIT-ASY-0127
FDA Recall
Terminated
·BioFire Diagnostics, LLC·Product code PEN·July 20, 2021
Sterile Disposable Kit ( Contains Skin Tensioner ASY-25067; Three Mark Needle Assembly ASY-25094; Nose Cone Assembly ASY-25098; Dissection 4 mm PRT-25117, follicle Trap PRT 23999): Product Usage: Skin Tensioner is applied to patients scalp during follicular harvesting during hair restoration procedure. Product applies tension to scalp to facilitate follicular extractions.
FDA Recall
Terminated
·Restoration Robotics·Product code ONA·October 13, 2013
FilmArray Pneumonia Panel (Pneumo) Part Numbers: Part No: RFIT-ASY-0144 / UDI: 00815381020178 (30 test kit) Part No: RFIT-ASY-0145 / UDI: 00815381020185 (6 test kit)
FDA Recall
Terminated
·BioFire Diagnostics, LLC·Product code QBH·June 7, 2021
FilmArray Pneumonia Panel plus (Pneumoplus) Part Numbers: Part No: RFIT-ASY-0143 / UDI: 00815381020314 (30 test kit) Part No: RFIT-ASY-0142 / UDI: 00815381020321 (6 test kit)
FDA Recall
Terminated
·BioFire Diagnostics, LLC·Product code QDS·June 7, 2021
Pathfast D-Dimer, Reference number: PF1051-KUS
FDA Recall
Terminated
·Lsi Medience Corporation 13-4 Uchikanda·Product code GHH·August 16, 2016
ASY, Brat 2 Procedure Set
FDA Recall
Terminated
·Cobe Cardiovascular, Inc·Product code CAC·June 22, 2005
ASY Brat 2 Procedure Set
FDA Recall
Terminated
·Cobe Cardiovascular, Inc·Product code CAC·June 22, 2005
ASY, Brat Pack Procedure Set
FDA Recall
Terminated
·Cobe Cardiovascular, Inc·Product code CAC·June 22, 2005
ASY Brat 2 Procedure Set
FDA Recall
Terminated
·Cobe Cardiovascular, Inc·Product code CAC·June 22, 2005
Affirm Lateral Arm Upright Biopsy Accessory. Product Number: ASY-09880
FDA Recall
Terminated
·Hologic, Inc.·Product code OIJ·July 7, 2017
ASY, Brat 2 Pack Procedure Set
FDA Recall
Terminated
·Cobe Cardiovascular, Inc·Product code CAC·June 22, 2005
Gram-Negative Bacteria And Associated Resistance Markers; Film Array Blood Culture Identification (BCID); Film Array BCID Panel - Product Usage: intended for use with FilmArray systems. Part No: RFIT-ASY-0126 / UDI: 00815381020086 Part No: RFIT-ASY-0127 / UDI: 00815381020093 IVD, Rx Only
FDA Recall
Terminated
·BioFire Diagnostics, LLC·Product code PEN·January 26, 2021
FilmArray BCID Panel (Blood Culture Identification Panel), Catalog numbers RFIT-ASY-0126 (30 test kit) and RFIT-ASY-0127 (6 test kit), when used with all lots of BD BACTEC Blood Culture Bottles, Catalog numbers 442020, 442021, 442023, 442192, 442265, 442194, 442022, 442193, 442260, and 442191.
FDA Recall
Terminated
·BioFire Diagnostics, LLC·Product code PEN·March 14, 2018
FilmArray BCID Panel, IVD, Rx Only, BioFire Diagnostics, REF: RFIT-ASY-0126, and RFIT-ASY-0127, when used with the following blood culture bottles: Bottle Description/Part Number: BACT/ALERT FA Plus/410851; BACT/ALERT FN Plus/410852; BACT/ALERT PF Plus/410853
FDA Recall
Terminated
·BioFire Diagnostics, LLC·Product code PEN·March 7, 2019