ABFLEX

GUDID 00850006892754

Abdominal Training Belt

WEB DEALS DIRECT LLC

Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use

• Primary Device ID: 00850006892754
• NIH Device Record Key: aeec2be1-78c3-42ed-bb52-0abf5299407b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ABFLEX
• Version Model Number: MC0485
• Company DUNS: 834979762
• Company Name: WEB DEALS DIRECT 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: false
• Manufacturing Date: false
• 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

Customer Support Contacts

• Phone: 800.930.2604
• Email: info@webdealsdirect.com
• Phone: 800.930.2604
• Email: info@webdealsdirect.com
• Phone: 800.930.2604
• Email: info@webdealsdirect.com
• Phone: 800.930.2604
• Email: info@webdealsdirect.com
• Phone: 800.930.2604
• Email: info@webdealsdirect.com
• Phone: 800.930.2604
• Email: info@webdealsdirect.com
• Phone: 800.930.2604
• Email: info@webdealsdirect.com
• Phone: 800.930.2604
• Email: info@webdealsdirect.com
• Phone: 800.930.2604
• Email: info@webdealsdirect.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850006892754 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K183103

FDA Product Code

• NGX: Stimulator, Muscle, Powered, For Muscle Conditioning

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: 2021-08-30
• Device Publish Date: 2021-08-20