LOGIQ

GUDID 00840682138260

GE MEDICAL SYSTEMS, ULTRASOUND & PRIMARY CARE DIAGNOSTICS, LLC

General-purpose ultrasound imaging system

• Primary Device ID: 00840682138260
• NIH Device Record Key: 97a6b755-8bed-4787-b59a-4b70cb3da520
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LOGIQ
• Version Model Number: E10
• Company DUNS: 078863378
• Company Name: GE MEDICAL SYSTEMS, ULTRASOUND & PRIMARY CARE DIAGNOSTICS, LLC
• 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

Device Dimensions

• Width: 585 Millimeter

Operating and Storage Conditions

• Handling Environment Temperature: Between -20 Degrees Celsius and 60 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840682138260 [Primary]

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: 2
• Public Version Date: 2018-05-23
• Device Publish Date: 2018-02-27

On-Brand Devices [LOGIQ]

• 00840682138260: E10
• 00840682120173: E9 R3 to R4 UPG
• 00840682120159: E9 R4 to R5 UPG
• 00840682102421: E9 R3 to XDclear 2.0 UPG
• 00840682102414: E9 R5 to XDclear 2.0 UPG
• 00840682102407: E9 R4 to XDclear 2.0 UPG
• 00840682102377: E9
• 00840682145640: E10 R2
• 00195278384041: LOGIQ E10 R3 Console
• 00195278680938: LOGIQ E10 R4 Console