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The Extech BR150 Video Borescope Inspection Camera, 9mm camera diameter and 2.4″ Color LCD Monitor feature a 2.4 in. color TFT LCD Monitor and a mini water-proof (IP67) 9 mm camera head with a dual light system for high resolution, glare-free, close-up viewing. Gooseneck cable retains configured shape. Detachable display for easy storage. Comes with 4 AA batteries, extension tools (mirror, hook, and magnet), video output jack, and hard case.
The Zistos Large Gun and Mortar Video Borescope is designed to replace the M3 Borescope used in the US and foreign militaries for artillery tube inspections over the past 30+ years. The dual camera (front and side view) video solution provides both an overview and detailed view of the condition of the inside of artillery tubes. A built in DVR can record video (AVI) and still (JPEG) images from the push of a button for reports, archival data, and for near real time transmission (email, etc.) to technical experts as needed. The simple to assemble and use kit is provided in a single waterproof transport case and is rugged and field proven for deployment as needed where needed.
Data for identification of the tube under inspection, and information about the location of what is under inspection (angle, depth, serial number, etc.) are recorded with the video or still pictures taken. A digital grid overlay, calibrated for each tube diameter is provided in order to estimate the size of artifacts found inside the tubes. A single operator can comfortably perform an inspection in a relatively compact area. The system can be run from a variety of power sources for maximum portability. Data can be transferred via removable SD flash card or through a host USB port to compatible external drives and flash media. Video and Still images can be reviewed on the DVR with no external display devices required.
Used with the Zistos Video Borescope system, the Digital Bore Measurement accessory replaces Pullover Gauges, STAR Gauge, and other bore gauges currently used to measure bore diameters on 57mm through 155mm artillery tubes. The digital bore measurement reading is captured on the Borescope video/stills along with other relevant tube data and visual observation of the measurement area. Measurements are straightforward to obtain and are accurate to better than – /+0.001” [-/+0.025mm] with minimally skilled operators. Measurements are ‘zeroed’ with included calibration rings for each bore of interest – effectively calibrated with each use. The same technique is utilized for all tubes thus simplifying training and deployment and logistics of various different measurement devices.
“Olympus’ highest priority is providing patients and users with safe and effective medical devices that comply with all applicable legal and regulatory requirements,” the company said in a statement to Medical Design & Outsourcing. “For that reason, we are committed to working together with FDA to address concerns.”
FDA issued the first letter to Aizu Olympus President and CEO Yasuo Takeuchi on Nov. 2, 2022, following a July 5–8 inspection. The warning letter covers the company’s endoscope and automated reprocessing equipment manufacturing operations in Aizuwakamatsu, Fukushima, Japan.
FDA issued the second letter to Olympus Medical Systems President Tomohisa Sakurai on Dec. 12, 2022, following a Sept. 6-9 inspection. That warning letter covers the company’s gastrointestinal and surgical endoscope manufacturing operations in Hachioji-shi, Tokyo, Japan.
FDA Center for Devices and Radiological Health (CDRH) Director Dr. Jeff Shuren said the agency and Olympus have “extensive and ongoing efforts” to address compliance issues related to the reprocessing of endoscopes.
“However, as described in the recent warning letters, Olympus is not in compliance with MDR reporting and quality system requirements,” Shuren said in a statement. “During recent inspections, CDRH determined that Olympus did not meet requirements to assure the quality and performance of the devices such as adequate testing and documentation of the device assembly process. In addition, Olympus did not develop MDR procedures, and did not submit MDRs within the required timeframes.”
More about the warning letter
Olympus makes, among many other products, surgical and gastrointestinal endoscopes and automated endoscope reprocessors. Endoscopes can be reused if appropriately cleaned and disinfected or sterilized to remove bacteria that could cause harmful or even fatal infections.
In its warning letter to Olympus Medical Systems, the FDA said the manufacturer conducted a device recall after receiving complaints that its uretero-reno fiberscope and uretero-reno videoscope malfunctioned while in use, but failed to notify the FDA as required by law. According to the FDA, Olympus responded with a promise to improve its MDR reporting process and train staff. The FDA said it could not determine the adequacy of that ongoing effort until its conclusion. A lot of us include the importance of an affiliate site. Gemstone for the purpose of exclusive and / or industry wearing, making your blog is definitely a especially tricky not to mention unnerving chore for the not really acquainted with code not to mention the different computer saavy portions of building a internet site. The conventional potential customer requirements as a way to source his or her's data files not to mention emerged accompanied by a web blog they could be especially excited to point out. One may suppose you need a power wand as a way to accomplish this task. Most certainly, please let an affiliate site initiator turn out to be who power wand.
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