Tri-Electrode Surface EMG

GUDID 00890477000395

SRS Medical Systems, Inc.

Cystometer

• Primary Device ID: 00890477000395
• NIH Device Record Key: 1c47f35d-3cf7-4b16-b729-6dc0501a683e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tri-Electrode Surface EMG
• Version Model Number: 730-003
• Company DUNS: 796263598
• Company Name: SRS Medical Systems, Inc.
• Device Count: 1
• 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: false
• Expiration Date: true
• 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	00890477000395 [Primary]
GS1	00890477000401 [Package]; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• EXQ: Cystometer, Electrical Recording

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: 2026-03-31
• Device Publish Date: 2026-03-04

On-Brand Devices [Tri-Electrode Surface EMG]

• 00089047700395: 730-003
• 00890477000395: 730-003