The brand name is the name that is typically registered with USPTO and have the ® and/or TM symbol.Braemar Shipping Services Plc engages in the knowledge and skill-based services to the shipping, marine, energy, offshore, and insurance industries. This information may 1) be on a label attached to a durable device, 2) be on a package of a disposable device, or 3) appear in labeling materials of an implantable device. Single Family, Condos, Multi-Family.The Proprietary/Trade/Brand name of the medical device as used in device labeling or in the catalog. General contractors and local builders are welcome to contact us to learn more about our mini storage building kits.Single Family Condos Multi-Family Commercial Land Rentals Mobile Home Apartment Farm Manufactured Townhouse.
See 21 CFR 807.3(b) for exceptions. The version or model identifies all devices that have specifications, performance, size, and composition within limits set by the labeler.The catalog, reference, or product number found on the device label or accompanying packaging to identify a particular product.Additional relevant information about the device that is not already captured as a distinct GUDID data attribute.Indicates the date the DI Record is published and available via Public Search.Indicates the date the device is no longer held or offered for sale by the labeler on record. The address is 3890 Canyon Corp Ctr Suite 100, San Diego, CA 92123.The version or model found on the device label or accompanying packaging used to identify a category or design of a device. The Shipbroking segment provides market access, operational support, strategic advice, and vess.Braemar Manufacturing LLC (Certificate 2014018033) is a business with business tax certificate issued by City of San Diego, Treasurer-Tax Collector.
Braemar Manufacturing Software Version That
This number is required to be part of the UDI when included on the label in order to provide the means to track the device back to its manufacturing source or otherwise allow the history of the device manufacturing, packaging, labeleing, distribution and use to be determined.The number that allows for the identification of a device, indicating its position within a series. At least one of the products in the combination product must be a device in this case.Indicates that the device is intended for one use or on a single patient during a single procedure.The number assigned to one or more device(s) that consist of a single type, model, class, size, composition, or software version that are manufactured under essentially the same conditions and that are intended to have uniform characteristics and quality within specified limits. Kits are a collection of products, including medical devices, that are packaged together to achieve a common intended use and is being distributed as a medical device.Indicates that the product is comprised of two or more regulated products that are physically, chemically, or otherwise combined or mixed and produced as a single entity packaged together as a single package or packaged separately for the intended use together as defined under 21 CFR 3.2(e). 3.Indicates that the device is a convenience, combination, in vitro diagnostic (IVD), or medical procedure kit.
Only applicable to devices not subject to the requirements under 21 CFR 801.437. Choosing 'Yes' indicates that the device label or packaging contains one of the following statements: (1) "Caution: This Product Contains Natural Rubber Latex Which May Cause Allergic Reactions", (2) This Product Contains Dry Natural Rubber", (3) Caution: The Packaging of This Product Contains Natural Rubber Latex Which May Cause Allergic Reactions" or (4) "The Packaging of This Product Contains Dry Natural Rubber".Device labeled as "Not made with natural rubber latex"Indicates that natural rubber latex was not used as materials in the manufacture of the medical product and container and the device labeling contains this information. This number/code is required to be part of the UDI when included on the label in order to provide the means to track the device back to its manufacturing source or otherwise allow the history of the device manufacturing, packaging, labeleing, distribution and use to be determined.Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)Indicates that the device or packaging contains natural rubber that contacts humans as described under 21 CFR 801.437. This date is required to be part of the UDI when included on the label in order to provide the means to track the device back to its manufacturing source or otherwise allow the history of the device manufacturing, packaging, labeleing, distribution and use to be determined.The Donation Identification Number is applicable to devices that are also regulated as HCT/Ps and is a number that is assigned to each donation. This date is required to be part of the UDI when included on the label in order to provide the means to track the device back to its manufacturing source or otherwise allow the history of the device manufacturing, packaging, labeleing, distribution and use to be determined.The date by which the label of a device states the device must or should be used.
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