AQUASONIC 100 01-02-1

GUDID 30855683006037

AQUASONIC 100, 60G TUBE

PARKER LABORATORIES INC

Electrode conductive medium

• Primary Device ID: 30855683006037
• NIH Device Record Key: d25a121e-35a2-4289-ade8-07ac87d8604f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AQUASONIC 100
• Version Model Number: ULTRASOUND TRANSMISSION GEL
• Catalog Number: 01-02-1
• Company DUNS: 002449593
• Company Name: PARKER LABORATORIES INC
• Device Count: 200
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 973-276-9500
• Email: customerservice@parkerlabs.com
• Phone: 973-276-9500
• Email: customerservice@parkerlabs.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00855683006036 [Unit of Use]
GS1	30855683006037 [Primary]

FDA Product Code

• MUI: Media,Coupling,Ultrasound

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: 2018-10-22
• Device Publish Date: 2017-07-05

On-Brand Devices [AQUASONIC 100]

• 00855683006531: AQUASONIC 100 ULTRASOUND TRANSMISSION GEL 5L
• 30855683006044: AQUASONIC 100 ULTRASOUND TRANSMISSION GEL 0.25L
• 30855683006037: AQUASONIC 100, 60G TUBE