Iogel Medium 2.5 cc electrode, Box of 12

GUDID 00888912151412

EMPI, INC.

Drug-delivery iontophoresis patch

• Primary Device ID: 00888912151412
• NIH Device Record Key: f7a635bc-6933-4b44-a43e-fb914535c72b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Iogel Medium 2.5 cc electrode, Box of 12
• Version Model Number: 5000022
• Company DUNS: 039375910
• Company Name: EMPI, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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: 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 Identifiers

Device Issuing Agency	Device ID
GS1	00888912151412 [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: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2014-09-24

Devices Manufactured by EMPI, INC.

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• 00888912151252 - Kit, Hybresis Controller: 2018-03-29
• 00888912151269 - Hybresis Iontophoresis Patch, Medium/Standard, Box of 6: 2018-03-29
• 00888912151283 - Action Patch Electrode ~ box of 4: 2018-03-29
• 00888912151290 - Iontophoresis Electrode Small 2.0 mL 3.75"x2.25" Box of 12: 2018-03-29
• 00888912151306 - Iontophoresis Electrode Medium 2.0 mL 3"x3" Box of 12: 2018-03-29