Hypoallergenic Electrode 2x2 4pk

GUDID 00085971800729

Emsi

Transcutaneous electrical stimulation electrode, single-use

• Primary Device ID: 00085971800729
• NIH Device Record Key: 711f9d0c-46e1-44f8-b90e-7fcf9d881a8f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hypoallergenic Electrode 2x2 4pk
• Version Model Number: BF5050
• Company DUNS: 932471881
• Company Name: Emsi
• 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	00085971800729 [Primary]

FDA Product Code

• GXY: Electrode, Cutaneous

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: 2024-08-26
• Device Publish Date: 2024-08-18

On-Brand Devices [Hypoallergenic Electrode 2x2 4pk]

• 00085971800729: BF5050
• 00859718007296: BF5050