Carbon Fiber Base Board, Long

GUDID B365501070

Aktina Corp.

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• Primary Device ID: B365501070
• NIH Device Record Key: 6fb881b3-de1f-4285-990a-10b9d2554b51
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Carbon Fiber Base Board, Long
• Version Model Number: 50-107
• Company DUNS: 787178920
• Company Name: Aktina Corp.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B365501070 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K103616

FDA Product Code

• IYE: Accelerator, Linear, Medical

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-05-31
• Device Publish Date: 2021-05-21

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