Transducer C5-2

GUDID 00884838072312

Philips Ultrasound, Inc.

Extracorporeal ultrasound imaging transducer, hand-held

• Primary Device ID: 00884838072312
• NIH Device Record Key: fc0d13fe-7e16-46a7-baed-f98bbe037ed6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Transducer C5-2
• Version Model Number: 989605451181
• 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	00884838072312 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K163020

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: 2018-11-12
• Device Publish Date: 2017-03-17

On-Brand Devices [Transducer C5-2]

• 00884838080713: 989605463361
• 00884838080706: 989605463351
• 00884838075672: 989605462851
• 00884838072312: 989605451181
• 00884838068766: 989605450352
• 00884838068018: 989605430242
• 00884838067424: 989605454101
• 00884838061828: 989605450351
• 00884838061804: 989605358813
• 00884838061385: 989605389242