Profile: Micro Power Electronics, Inc. provides custom battery systems to the portable medical, automatic data collection and commercial military markets. We offer power solutions for portable applications. We design medical batteries and battery chargers for medical equipments such as defibrillators (AED), ultrasound devices, patient monitoring equipment, multi-parameter monitors, critical care monitors, infusion pumps, endoscopes, portable X-ray, intra-aortic balloon pumps (IABP), ventilators and surgical instruments.
The company has revenues of USD 25-50 Million, has ~250 employees and is ISO 13485, ISO 9001: 2000 certified. NASDAQ:CBAK. (SEC Filings)
FDA Registration Number: 3032867
2 Products/Services (Click for related suppliers)
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• Battery |
• Rechargeable Battery Box (FDA Code: FCO / 876.1500) An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals. The device consists of various rigid or flexible instruments that are inserted into body spaces and may include an optical system for conveying an image to the user's eye and their accessories may assist in gaining access or increase the versatility and augment the capabilities of the devices. Examples of devices that are within this generic type of device include cleaning accessories for endoscopes, photographic accessories for endoscopes, nonpowered anoscopes, binolcular attachments for endoscopes, pocket battery boxes, flexible or rigid choledochoscopes, colonoscopes, diagnostic cystoscopes, cystourethroscopes, enteroscopes, esophagogastroduodenoscopes, rigid esophagoscopes, fiberoptic illuminators for endoscopes, incandescent endoscope lamps, biliary pancreatoscopes, proctoscopes, resectoscopes, nephroscopes, sigmoidoscopes, ureteroscopes, urethroscopes, endomagnetic retrievers, cytology brushes for endoscopes, and lubricating jelly for transurethral surgical instruments. This section does not apply to endoscopes that have specialized uses in other medical specialty areas and that are covered by classification regulations in other parts of the device classification regulations. |