Newyork, Feb. 07, 2023 (GLOBE NEWSWIRE) -- According to a newly released Persistence Market Research study, the Surgical Instrument Tracking System Market sales were assessed at US$ 208.6 Million ...

Fonon Technologies , a pioneer in next-generation 3D Fiber and CO2 Material Processing Systems, announces its LaserTower™ family of FDA compliant permanent UDI marking systems for medical device ...

121nexus Scanner App instantaneously reads healthcare barcodes and delivers device-specific information including FDA's GUDID database (GUDID) and product specific information from integrated ...

Under 21 CFR 801.20, a UDI is required on the label and package of every medical device in commercial distribution in the United States (unless an exception or alternative applies).

While UDI labeling requirements will be phased in through 2020, all labels and packages of Class II medical devices must have UDI barcodes starting Sep. 24. Here are four things to know about the ...

Today, a UDI is required on labels and packaging for all FDA-rated Class III devices—the highest-risk devices on the market because their failure could be life-threatening—and all implantable ...