BodyMed Iontophoresis Electrode Kit

GUDID 10853904006053

Compass Richmar, LLC

Drug-delivery iontophoresis patch

• Primary Device ID: 10853904006053
• NIH Device Record Key: a16a19d1-969c-42ad-9072-00020a4c29bd
• Commercial Distribution Discontinuation: 2023-09-22
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: BodyMed Iontophoresis Electrode Kit
• Version Model Number: Medium, Box of 12
• Company DUNS: 080930531
• Company Name: Compass Richmar, 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: true
• 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	10853904006053 [Primary]

FDA Product Code

• EGJ: Device, Iontophoresis, Other Uses

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: 2023-09-25
• Device Publish Date: 2016-05-02

On-Brand Devices [BodyMed Iontophoresis Electrode Kit]

• 00853904006070: Butterfly (3.75"x3.75")
• 00853904006063: Large (3.5"x3.5")
• 00853904006056: Medium (3.25"x3.25")
• 00853904006049: Small (2.75"x2.75")
• 10853904006077: Butterfly, Box of 12
• 10853904006060: Large, Box of 12
• 10853904006053: Medium, Box of 12
• 10853904006046: Small, Box of 12