EasyFlo Console

GUDID 00890477000364

SRS Medical Systems, Inc.

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• Primary Device ID: 00890477000364
• NIH Device Record Key: 781edb6a-e5f9-4130-9d60-3a6453f650ac
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EasyFlo Console
• Version Model Number: 900-044
• 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	00890477000364 [Primary]

FDA Product Code

• EXY: Uroflowmeter

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: 2023-05-04
• Device Publish Date: 2023-04-26

Devices Manufactured by SRS Medical Systems, Inc.

• 00890477000364 - EasyFlo Console: 2023-05-04
• 00890477000364 - EasyFlo Console: 2023-05-04
• 00890477000166 - Discovery Base Unit: 2022-11-28
• 00890477000074 - Insight Discovery Thermal: 2021-08-30
• 00890477000081 - Insight Discovery PWP: 2021-08-30
• 00890477000104 - Insight Discovery Dual Inclinometer: 2021-08-30
• 00890477000159 - Insight Discovery Algometer: 2021-08-30
• 00890477000173 - Insight Discovery PWP (w/cable): 2021-08-30
• 00890477000180 - EMG Sensor: 2021-08-30