7,350 results · 13ms · 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.

Pointts sistema de ellmlnact!;o de verrugas OTC - Brazil Catalog Number: 1001-0280 - Product Usage: indicated for over-the-counter a cryosurgical system for the treatment of skin tags.

FDA Enforcement
Class III ·Terminated·OraSure Technologies, Inc.·September 30, 2020

Pointts sistema de ellmlnact!;o de verrugas OTC - Brazil Catalog Number: 1001-0280 - Product Usage: indicated for over-the-counter a cryosurgical system for the treatment of skin tags.

FDA Recall
Terminated ·OraSure Technologies, Inc.·Product code GEH·July 15, 2020

Cirugia Cardiovascular Case Cart, c ode 900-1415A, contains: (1) CIRUGIA CARDIOVASCULAR .(INDUCCION) (1) CIRUGIA CARDIOVASCULAR (CIRUGIA ) (1) CIRUGIA CARDIOVASCULAR (PREP ENFERMERA CIRCULANTE) (1) CIRUGIA CARDIOVASCULAR (PERFUSION SUPPLIES) (1) CIRUGIA CARDIOVASCULAR (POST- CIRUGIA) (1) OPEN HEART TRAY Product Usage: EO sterilized surgical convenient packs packaged into polyester/polyethylene breather bag with Tyvek double vents.

FDA Enforcement
Class I ·Terminated·Customed, Inc·September 10, 2014

Cirugia Cardiovascular Case Cart, c ode 900-1415A, contains: (1) CIRUGIA CARDIOVASCULAR .(INDUCCION) (1) CIRUGIA CARDIOVASCULAR (CIRUGIA ) (1) CIRUGIA CARDIOVASCULAR (PREP ENFERMERA CIRCULANTE) (1) CIRUGIA CARDIOVASCULAR (PERFUSION SUPPLIES) (1) CIRUGIA CARDIOVASCULAR (POST- CIRUGIA) (1) OPEN HEART TRAY Product Usage: EO sterilized surgical convenient packs packaged into polyester/polyethylene breather bag with Tyvek double vents.

FDA Recall
Terminated ·Customed, Inc Calle Igualdad Final # 7·Product code OFA·May 20, 2014

EndoGastric Solutions EsophyX2 Plus Device with Serosa Fastener and Accessories Part number C02033-01. Label reads in part "EsophyX2 2-LINK Device Qty: (1) Fastener Delivery System ***" Designed for the treatment of Gastroesophageal Reflux Disease (GERD), with erosive and non-erosive esophagitis

FDA Recall
Terminated ·Endogastric Solutions Inc·Product code ODE·February 4, 2013

EndoGastric Solutions EsophyX2 Device with Serosa Fastener and Accessories. Models R2001 and R2002. Indicated for the treatment of symptomatic chronic gastroesophageal reflux disease.

FDA Recall
Terminated ·Endogastric Solutions Inc·Product code ODE·June 6, 2013

LifeSync ECG System - Disposable leadwear, Ls-222, Ls-223

FDA Recall
Terminated ·GMP Companies/Lifesync Corporation·Product code DRG·January 10, 2007

BioSentry Tract Sealant System, Product Code: 768022019S; Indicated to provide accuracy in marking a biopsy location for visualization during surgical resection.

FDA Enforcement
Class II ·Terminated·Surgical Specialties Mexico S DE RL DE CV·October 19, 2016

iba COMPASS SW Version 3.0, Catalog Number CS10-100 (medical linear accelerator) radiological

FDA Recall
Terminated ·Iba Dosimetry Gmbh Bahnhofstr. 5 Schwarzenbruck Germany·Product code IYE·August 20, 2013

HEPFLUSH-10 (HEPARIN LOCK FLUSH SOLUTION, USP) 100 USP units per 10 mL (10 USP units per mL), Single Dose Vial, Rx only -- Fresenius Kabi USA, LLC -- NDC 63323-017-10, Product Code 1710

FDA Recall
Terminated ·Fresenius Kabi USA, LLC·Product code NZW·December 19, 2014

Spectrum IQ - Infusion Pump - Product Usage: intended to be used for the controlled administration of fluids.

FDA Recall
Terminated ·Baxter Healthcare Corporation·Product code FRN·March 19, 2021

BioSentry Tract Sealant System, Product Code: 768022019S; Indicated to provide accuracy in marking a biopsy location for visualization during surgical resection.

FDA Recall
Terminated ·Surgical Specialties Mexico S DE RL DE CV Corredor Tijuana Rosarito 2000-24702 B Ejido Francisco Villa Tijuana Mexico·Product code OMT·September 24, 2016

3mL 9NC Coagulation Sodium Citrate 3.2%, Item #454334, Greiner Bio-One North America Inc., 4238 Capital Drive, Monroe, NC 28110. Intended Use: Venous blood collection tubes.

FDA Enforcement
Class II ·Terminated·Greiner Bio-One North America, Inc.·August 15, 2012

VACUETTE TUBE, 3.5mL CAL Serum Sep Clot Activator, REF 454067P - Product Usage: VACUETTE Tubes, Holders, and Needles are use together as a system for the collection of venous blood. VACUETTE tubes are used to collect, transport, and process blood for testing serum, plasma, or whole blood in the clinical laboratory.

FDA Enforcement
Class II ·Terminated·Greiner Bio-One North America, Inc.·January 29, 2020

VACUETTE Tube 2ml 9NC Coagulation Sodium Citrate 3.2%. Item no. 454322. Lot no. B1908355.

FDA Enforcement
Class II ·Terminated·Greiner Bio-One North America, Inc.·April 22, 2020

Greiner Bio-One VACUETTE¿ TUBE 2 ml 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube, non-ridged

FDA Enforcement
Class II ·Terminated·Greiner Bio-One North America, Inc.·September 29, 2021

Vacuette Quickshield Complete Plus, 21G x 1 (0.8 x 25 mm), Greiner bio-one. The Quick shield Complete Plus is intended to be used only with Vacuette Blood collection Tubes as a system in routine venipuncture procedures. They are for single-use only and should only be used by adequately trained healthcare personnel in accordance with instructions for use.

FDA Enforcement
Class II ·Terminated·Greiner Bio-One North America, Inc.·July 11, 2012

4 ml FX Sodium Fluoride/Potassium Oxalate tube, Ref 454297 VACUETTE Glycolytic Inhibitor Tubes contain an antiglycolytic agent, sodium fluoride, and an anticoagulant, potassium oxalate. The product is suitable for the analysis of blood glucose and lactate

FDA Enforcement
Class II ·Terminated·Greiner Bio-One North America, Inc.·June 15, 2016

VACUETTE Safety Blood Collection Set + Luer Adapter, 23x12" Safety Blood Collect LA Product, Item number 450096. Usage: The Safety Blood Collection Set is used in routine venipuncture procedures.

FDA Enforcement
Class II ·Terminated·Greiner Bio-One North America, Inc.·February 27, 2013

VACUETTE TUBE 5 mL CAT Serum Separator Clot Activator, Item Number: 456018P - Product Usage: are used to collect, transport, and process blood for testing serum, plasma or whole blood in the clinical laboratory.

FDA Enforcement
Class II ·Terminated·Greiner Bio-One North America, Inc.·October 7, 2020