Electrode Skin Prep Pads

GUDID 00810180842716

Dynarex Corporation

Electrode skin abrasion pad

• Primary Device ID: 00810180842716
• NIH Device Record Key: cc2a4b7f-f19d-4108-a58d-90517e8e4574
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Electrode Skin Prep Pads
• Version Model Number: 1508
• Company DUNS: 008124539
• Company Name: Dynarex Corporation
• Device Count: 100
• 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: false
• 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	00616784150826 [Primary]
GS1	00616784150833 [Package]; Contains: 00616784150826; Package: Case [10 Units]; In Commercial Distribution
GS1	00810180842716 [Unit of Use]

FDA Product Code

• KOY: Degreaser, Skin, Surgical

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2026-02-17
• Device Publish Date: 2022-05-10

On-Brand Devices [Electrode Skin Prep Pads]

• 00616784150819: 1508
• 00810180842716: 1508