LOGIQ

GUDID 00840682105392

GE Medical Systems (China) Co.,Ltd.

General-purpose ultrasound imaging system

• Primary Device ID: 00840682105392
• NIH Device Record Key: 2c6c2155-1452-4e2c-86ef-586f0ecd0ea6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LOGIQ
• Version Model Number: e R6 to R7 UPG
• 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

Customer Support Contacts

• Phone: +1(800)437-1171
• Email: xx@xx.xx

Operating and Storage Conditions

• Storage Environment Temperature: Between -5 Degrees Celsius and 50 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840682105392 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K151028

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: 4
• Public Version Date: 2018-07-06
• 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