Registrar Corp

HomeMedical DevicesRegistration & Medical Device ListingsMedical Device Samples › U.S. FDA Pocket Battery Boxes Regulations

U.S. FDA Medical Device Pocket Battery Boxes Requirements

FDA Medical Device Definition: 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.

Registrar Corp assists Pocket Battery Boxes companies with:

  • FDA Pocket Battery Boxes Establishment Registration
  • FDA Pocket Battery Boxes Listing
  • FDA Pocket Battery Boxes Label Requirements and Exceptions
  • FDA Pocket Battery Boxes Import Information
  • FDA Pocket Battery Boxes Detentions (Pocket Battery Boxes Entry Refusals)
  • General U.S. Food and Drug Administration Medical Device Guidelines for:
       - Pocket Battery Boxes Manufacturers (Pocket Battery Boxes Suppliers)
       - Pocket Battery Boxes Distributors
       - Pocket Battery Boxes Processors
       - Pocket Battery Boxes Repackers
       - Pocket Battery Boxes Relabelers
       - Pocket Battery Boxes Exporters
       - Pocket Battery Boxes Importers
For more information about Pocket Battery Boxes Medical Devices, simply click below:

U.S. FDA Regulations:

U.S. FDA 510(k) Regulation: 21 C.F.R. section 814.9.

Registrar Corp assists businesses with U.S. FDA compliance. Certificates of Registration issued by Registrar Corp provide confirmation to industry that you are fulfilling U.S. FDA registration requirements. U.S. FDA does not issue or recognize Certificates of Registration. Registrar Corp is not affiliated with the U.S. Food and Drug Administration.
Home | About Us | News | Resources | Exhibitions | Seminars | Associations | Careers | Sitemap | Terms of Use © 2016 Registrar Corp
Food and Beverages | Drugs | Cosmetics | Medical Devices | Radiation-Emitting Electronic Devices | Color Additives | Tobacco