562 results · 20ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

Brand Name: MST Duet Reusable Handle for Single Use Heads Product Name: Reusable Handle for Single Use Heads (Forceps and Scissors) Model/Catalog Number: DFH-1028 Software Version: N/A Product Description: A MST Single Use Forceps or Scissors System consists of a reusable handle and one of a number of single use interchangeable heads. MST Single Use Forceps and Scissor heads are shipped ready to use sterile in a tray with Tyvek lid within a sterile pouch. MST Duet Reusable Handle for Single Use Forceps & Scissor Heads are supplied in a non-sterile condition and must be sterilized prior to and after every use. The blue sleeve the handle is packaged in is not intended to be sterilized and does not maintain sterility. Component: Yes. The MST Duet Reusable Handle for Single Use Heads is the reusable handle component which connect to either Single Use Forceps or Scissors heads.

FDA Recall
Open, Classified ·MicroSurgical Technology Inc·Product code HNF·September 17, 2024

Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved PG, Catalog Number 45-871

FDA Recall
Terminated ·Angiodynamics Inc. (Navilyst Medical Inc.)·Product code LJS·May 10, 2018

BioFlo Midline 5F DL-20cm MST-45 Kit w/ Two Nitinol Guidewires PG, Catalog Number 46-810

FDA Recall
Terminated ·Angiodynamics Inc. (Navilyst Medical Inc.)·Product code FOZ·May 10, 2018

Bio-Stable 5F SL-55CM MST-70 Kit Valved with Nitinol Guidewire PG, Catalog Number 45-892

FDA Recall
Terminated ·Angiodynamics Inc. (Navilyst Medical Inc.)·Product code LJS·May 10, 2018

Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved with Nitinol Guidewire PG, Catalog Number 45-895

FDA Recall
Terminated ·Angiodynamics Inc. (Navilyst Medical Inc.)·Product code LJS·May 10, 2018

MST ArcDUO 9mm, REF: ARC-0002, single-use, sterile ophthalmic knife, used with Suction Set, Part: 48-1000-01

FDA Recall
Open, Classified ·MicroSurgical Technology Inc·Product code HNN·August 20, 2025

EliA GliadinDP IgG Well in the Phadia 2500EE instrument (Material Number 12410002) EliA GliadinDP IgG is intended for the in vitro semi-quantitative measurement of IgG antibodies directed to gliadin in human serum or plasma (Li-heparin, EDTA) to aid in the diagnosis of celiac disease Material Number 14553901

FDA Recall
Open, Classified ·Phadia US Inc·Product code MST·May 1, 2023

Is-anti-Gliadin IgG Enzyme Immunoassay Test Kit packaged in cardboard boxes with individual components secured within a foam insert. Catalog Number # 720-800. - Laboratory In-Vitro Diagnostic Assay intended for the semi-quantitative detection of IgG antibodies to Gliadin in human serum by indirect enzyme immunoassay as an aid in the diagnosis of celiac disease.

FDA Recall
Terminated ·Diamedix Corporation·Product code MST·March 21, 2008

Phadia 2500EE instrument -Intended for the in vitro semi-quantitative measurement of IgG antibodies directed to gliadin in human serum or plasma (Li-heparin, EDTA) to aid in the diagnosis of celiac disease Material Number 12410002

FDA Recall
Open, Classified ·Phadia US Inc·Product code MST·May 1, 2023

Microsurgical Operating Room Tables;7300BX (18-351-70).

FDA Recall
Open, Classified ·Mizuho America, Inc.·Product code GDC·September 11, 2019

Microsurgical Operating Room Tables;7300B (18-350-70);

FDA Recall
Open, Classified ·Mizuho America, Inc.·Product code GDC·September 11, 2019

CRITIFLO(tm) FLUSH KIT

FDA Recall
Terminated ·Becton Dickinson Medical Systems·Product code KRA·July 1, 2005

CRITIFLO(tm) flush kit.

FDA Recall
Terminated ·Becton Dickinson Medical Systems·Product code KRA·July 1, 2005

TAKHPQ60R continuous flow catheter.

FDA Recall
Terminated ·Becton Dickinson Medical Systems·Product code KRA·July 1, 2005

DTX(tm) Plus DT-DL60 Continuous flush catheter

FDA Recall
Terminated ·Becton Dickinson Medical Systems·Product code KRA·July 1, 2005

DT-DL60-1 W/Bifurcated

FDA Recall
Terminated ·Becton Dickinson Medical Systems·Product code KRA·July 1, 2005

CRITIFLOW(tm) TA4004 continuous flush catheter

FDA Recall
Terminated ·Becton Dickinson Medical Systems·Product code KRA·July 1, 2005

CRITIFLO(tm) TAK0460 continuous flow catheter

FDA Recall
Terminated ·Becton Dickinson Medical Systems·Product code KRA·July 1, 2005

Cardinal Steam Biological Indicator, SteriTec Product Code PL 218, Distributor Product Code T40360EZ EZTest Steam Biological Indicator: Mesa EZTest Steam Biological Indicator is a self contained Biological Indicator intended for monitoring the efficacy of 121C, 132C, 134C and 135C steam sterilization cycles. Mesa EZTest has a recommended incubation time of 24 hours.

FDA Recall
Terminated ·Steritec Products Mfc. Co., Inc.·Product code FRC·June 10, 2013

Medline Steam Biological Indicators, SteriTec Product Code PL 353, Distributor Product Code MDS200525 EZTest Steam Biological Indicator: Mesa EZTest Steam Biological Indicator is a self contained Biological Indicator intended for monitoring the efficacy of 121C, 132C, 134C and 135C steam sterilization cycles. Mesa EZTest has a recommended incubation time of 24 hours.

FDA Recall
Terminated ·Steritec Products Mfc. Co., Inc.·Product code FRC·June 10, 2013