Goppli

GUDID 00850060516139

A&B Wholesale LLC

Skin topical coupling gel

• Primary Device ID: 00850060516139
• NIH Device Record Key: 8e2021a1-bbbe-49c8-b1ff-7e236ee34f54
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Goppli
• Version Model Number: GOPPUG250
• Company DUNS: 118927708
• Company Name: A&B Wholesale 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: true
• Serial Number: false
• Manufacturing Date: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850060516115 [Primary]
GS1	00850060516139 [Package]; Contains: 00850060516115; Package: Box [2 Units]; In Commercial Distribution

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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-04-29
• Device Publish Date: 2024-04-19

On-Brand Devices [Goppli]

• 00850060516122: GOPPUG5L
• 00850060516139: GOPPUG250