TMR-ELEC-20402321 1.9 x 3.75 WH, DLX Electrode

GUDID 00858688006605

Emsi

Transcutaneous electrical stimulation electrode

• Primary Device ID: 00858688006605
• NIH Device Record Key: ed6e67f3-d915-441e-b7f4-e85a7133ddc5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TMR-ELEC-20402321 1.9 x 3.75 WH, DLX Electrode
• Version Model Number: A2321
• 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: 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	00858688006605 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K050788

FDA Product Code

• GXY: Electrode, Cutaneous

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: 2018-07-06
• Device Publish Date: 2016-09-22

Devices Manufactured by Emsi

• 00085971800729 - Hypoallergenic Electrode 2x2 4pk: 2024-08-26
• 00858688006964 - Electrode 45 x 45 16 PK: 2023-09-28
• 00858688006971 - Electrode 1.75 x 1.75 4 pack: 2023-09-28
• 00859718007074 - Electrode 1.75 x 1.75 - 24 PK: 2023-09-28
• 00859718007081 - Electrode 4.0 x 7.0- Dispersive: 2023-09-28
• 00859718007098 - Electrode 1 Inch Round 4 PK: 2023-09-28
• 00859718007104 - Electrode 2" round 4pk: 2023-09-28
• 00859718007111 - Electrode 3 Inch Round 4PK: 2023-09-28