Philips Compatible NIBP Hose

GUDID B817AS161500

CABLES AND SENSORS, LLC

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• Primary Device ID: B817AS161500
• NIH Device Record Key: c8db6c99-433f-4bff-97bd-edc611d6b5a9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Philips Compatible NIBP Hose
• Version Model Number: AS-16-150
• Company DUNS: 040814020
• Company Name: CABLES AND SENSORS, LLC
• 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: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B817AS161500 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K173197

FDA Product Code

• DXQ: Blood Pressure Cuff

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: 2021-07-30
• Device Publish Date: 2021-07-22

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