LOGIQ

GUDID 00840682102933

GE Medical Systems (China) Co.,Ltd.

General-purpose ultrasound imaging system

• Primary Device ID: 00840682102933
• NIH Device Record Key: 1b158ecc-2d7a-4813-a1ab-3ce513f8c334
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LOGIQ
• Version Model Number: V2
• Company DUNS: 654658731
• Company Name: GE Medical Systems (China) Co.,Ltd.
• 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: true
• OTC Over-The-Counter: false

Operating and Storage Conditions

• Storage Environment Atmospheric Pressure: Between 70 KiloPascal and 106 KiloPascal

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840682102933 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K153037

FDA Product Code

• IYO: System, imaging, pulsed echo, ultrasonic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-08-13
• Device Publish Date: 2016-08-01

On-Brand Devices [LOGIQ]

• 00840682146913: e SW R9.1.X UPG
• 00840682146944: e SW R9.2.X UPG
• 00840682146081: e R8
• 00840682106924: V3
• 00840682106825: V5
• 00840682106658: V5 Expert
• 00840682105392: e R6 to R7 UPG
• 00840682103855: e
• 00840682103695: F8 Expert
• 00840682103657: F8
• 00840682103565: F6
• 00840682102940: V1
• 00840682102933: V2
• 00195278674203: LOGIQ e TB Standard Console
• 00195278674197: LOGIQ e TP Standard Console
• 00195278722430: Magna R3 LOGIQ F Basic console