PowerLook AMP SLD GE OUS Direct

GUDID 00858012005106

Icad, Inc.

Basic diagnostic x-ray system application software

• Primary Device ID: 00858012005106
• NIH Device Record Key: 8a80387a-f09c-451d-b570-376a5c74b029
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PowerLook AMP SLD GE OUS Direct
• Version Model Number: DSC010-12-EU
• Company DUNS: 108870254
• Company Name: Icad, 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: true
• 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	00858012005106 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P010038

FDA Product Code

• MYN: Analyzer, Medical Image

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-05-25
• Device Publish Date: 2021-05-17

Devices Manufactured by Icad, Inc.

• 00850008977053 - TESTING: 2024-06-18
• 00850008977251 - PowerLook Density Assessment V4.0: 2024-06-18
• 00850008977268 - ProFound AI 3.1: 2024-06-18
• 00850008977275 - ProFound AI 3.1: 2024-06-18
• 00850008977282 - TESTING: 2024-06-18
• 00850008977299 - PowerLook PRO+ 4GPU Tower Platform, OUS: 2024-06-18
• 00850008977305 - PowerLook 10.1.1: 2024-06-18
• 00850008977312 - PowerLook MammoAI Container - Sectra: 2024-06-18