Transducer L12-4

GUDID 00884838072305

Philips Ultrasound, Inc.

Extracorporeal ultrasound imaging transducer, hand-held

• Primary Device ID: 00884838072305
• NIH Device Record Key: 8721150b-96a3-40bc-aa44-904e03845fdb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Transducer L12-4
• Version Model Number: 989605451171
• 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	00884838072305 [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 L12-4]

• 00884838072305: 989605451171
• 00884838068759: 989605434812
• 00884838067882: 989605418963
• 00884838061835: 989605434811
• 00884838061644: 989605427122
• 00884838061484: 989605430652
• 00884838061408: 989605389262