Uroflow Scale

GUDID 00890477000203

SRS Medical Systems, Inc.

Cystometer Cystometer Cystometer Cystometer Cystometer Cystometer Cystometer Cystometer Cystometer

• Primary Device ID: 00890477000203
• NIH Device Record Key: d3f6f079-ce2b-40ab-93c6-25e763a42f30
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Uroflow Scale
• Version Model Number: 900-035
• 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: false
• Lot Batch: false
• Serial Number: true
• 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	00890477000203 [Primary]

FDA Product Code

• EXQ: Cystometer, Electrical Recording

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: 2021-08-27
• Device Publish Date: 2021-08-19

On-Brand Devices [Uroflow Scale]

• 00890477000357: 900-042
• 00890477000203: 900-035