WiFLOW WLC

GUDID 00852423006387

Uroflowmetry WiFLOW® System

PROMETHEUS GROUP OF NEW HAMPSHIRE LIMITED, THE

Urine flowmeter, reusable

• Primary Device ID: 00852423006387
• NIH Device Record Key: 47550973-0180-4262-a7af-aa1b922e026e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: WiFLOW
• Version Model Number: WI-LC
• Catalog Number: WLC
• Company DUNS: 625863568
• Company Name: PROMETHEUS GROUP OF NEW HAMPSHIRE LIMITED, THE
• 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: true
• 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

Customer Support Contacts

• Phone: 1.800.442.2325
• Email: info@theprogrp.com
• Phone: 1.800.442.2325
• Email: info@theprogrp.com
• Phone: 1.800.442.2325
• Email: info@theprogrp.com
• Phone: 1.800.442.2325
• Email: info@theprogrp.com
• Phone: 1.800.442.2325
• Email: info@theprogrp.com
• Phone: 1.800.442.2325
• Email: info@theprogrp.com
• Phone: 1.800.442.2325
• Email: info@theprogrp.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00852423006387 [Primary]

FDA Product Code

• EXY: Uroflowmeter

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: 2018-05-25
• Device Publish Date: 2017-02-14

Devices Manufactured by PROMETHEUS GROUP OF NEW HAMPSHIRE LIMITED, THE

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