Transducer C9-3v

GUDID 00884838024304

Philips Ultrasound, Inc.

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• Primary Device ID: 00884838024304
• NIH Device Record Key: c4b0c58d-5d52-43e0-93e8-88d456400169
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Transducer C9-3v
• Version Model Number: 989605366341
• Company DUNS: 063377717
• Company Name: Philips Ultrasound, Inc.
• 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: 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
GS1	00884838024304 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K030455

FDA Product Code

• IYO: System, imaging, pulsed echo, ultrasonic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-09-30
• Device Publish Date: 2016-10-28

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