MicroDose SI 714048

GUDID 00884838070943

Philips MicroDose Mammography SI L50 is intended to produce radiographic images of the human breast for the purpose of diagnostic and screening mammography. The system is intended to be used in the same clinical applications as traditional film-based mammography systems.

Philips Digital Mammography Sweden AB

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• Primary Device ID: 00884838070943
• NIH Device Record Key: 4614fee8-ebbd-4191-92cf-e74dfb702ec0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MicroDose SI
• Version Model Number: L50
• Catalog Number: 714048
• Company DUNS: 632899233
• Company Name: Philips Digital Mammography Sweden AB
• Device Count: 1
• DM Exempt: true
• 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: true
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884838070943 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K130704

FDA Product Code

• MUE: Full field digital,system,x-ray,mammographic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-11-12
• Device Publish Date: 2016-08-31

On-Brand Devices [MicroDose SI]

• 00884838071001: Philips MicroDose SI (Model: L50) is intended to produce radiographic images of the human breast
• 00884838070943: Philips MicroDose Mammography SI L50 is intended to produce radiographic images of the human bre