DL800 Patient Cable

GUDID B146DL800

BRAEMAR MANUFACTURING, LLC

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• Primary Device ID: B146DL800
• NIH Device Record Key: 9ad808bc-3364-460b-9b76-d5043873b73d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DL800 Patient Cable
• Version Model Number: 350-0235-00
• Company DUNS: 049529118
• Company Name: BRAEMAR MANUFACTURING, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• Manufacturing Date: false
• 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	B146DL800 [Primary]

FDA Product Code

• IKD: Cable, Electrode

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-10-21
• Device Publish Date: 2019-10-08

On-Brand Devices [DL800 Patient Cable]

• B146DL830: 350-0235-03
• B146DL800: 350-0235-00