L12-4 Transducer

GUDID 00884838085169

Philips Ultrasound, Inc.

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• Primary Device ID: 00884838085169
• NIH Device Record Key: e7d2cea9-430e-45d2-a3cc-0211084632c1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: L12-4 Transducer
• Version Model Number: 989605434813
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884838085169 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K162549

FDA Product Code

• ITX: Transducer, ultrasonic, diagnostic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-10-21

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