FDA

FDA (Food and Drug Administration) 注册是指在美国食品药品监督管理局注册或登记某种产品、设备或机构以合法地在美国市场销售、分发或生产。
Megadyne Reiterates Intended Use Population Change for Megadyne Mega Soft Universal and Universal Pl

SummaryCompany Announcement Date:February 29, 2024FDA Publish Date:February 29,

Wipro GE Healthcare Private Ltd. Recalls Care Plus, Care Plus models 1000-4000 and Lullaby Incubator

Please be aware, this recall is a correction, not a product removal.The FDA has

Smiths Medical ASD Inc. Recalls Medfusion Model 3500 Syringe Pump Due to Issues Associated with Earl

Please be aware, this recall is a correction, not a product removal.Recalled Pro

UPDATE: Evaluating Plastic Syringes Made in China for Potential Device Failures: FDA Safety Communic

Update: August 16, 2024While piston syringes manufactured by Zhejiang Longde Pha

Disruptions in Availability of BD BACTEC Blood Culture Media Bottles - Letter to Health Care Provide

Update: August 15, 2024The FDA updated this communication to add additional exte

Electrode Pad Correction: Megadyne Issues Correction for MEGA SOFT, MEGA SOFT DUAL and MEGA 2000 Pat

UPDATES:Starting in September 2024, Megadyne communicated in a letterExternal Li

Ambulatory Infusion Pump Software Correction: Smiths Medical Issues Correction for CADD-Solis and CA

This recall involves correcting certain devices, and does not involve removing t

Infusion Pump Battery Correction: ICU Medical Updates Instructions for Use Regarding Batteries in Pl

This recall involves updating instructions for using certain devices, and does n

Continuous Glucose Monitoring (CGM) Sensor Recall: Abbott Diabetes Care Inc Issues Recall for Certai

This recall involves removing certain devices from where they are used or sold,

Tracheostomy Tube Recall: Smiths Medical Removes Certain Bivona Neonatal/Pediatric and Adult Tracheo

This recall involves removing certain devices from where they are used or sold.

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