DL950 patient Cable

GUDID B146DL950

BRAEMAR MANUFACTURING, LLC

Electrocardiographic lead set, reusable

• Primary Device ID: B146DL950
• NIH Device Record Key: 319a768c-d8e6-4484-a661-d2d23117c74f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DL950 patient Cable
• Version Model Number: 350-0318-00
• 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	B146DL950 [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 [DL950 patient Cable]

• B146DL9510: 350-0318-01
• B146DL950: 350-0318-00