Pathway® NMR 200

GUDID 00852423006394

Pathway® NMR 200 Dual Channel Module

PROMETHEUS GROUP OF NEW HAMPSHIRE LIMITED, THE

Perineometer

• Primary Device ID: 00852423006394
• NIH Device Record Key: 13d9b44d-e919-4e0b-9678-7a47de6f3943
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pathway®
• Version Model Number: NMR 200
• Catalog Number: NMR 200
• Company DUNS: 625863568
• Company Name: PROMETHEUS GROUP OF NEW HAMPSHIRE LIMITED, THE
• 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: 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: false
• 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	00852423006394 [Primary]

FDA Product Code

• HIR: Perineometer

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: 2018-10-01
• Device Publish Date: 2018-08-30

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• 00852423006172: Pathway® 6330 Vaginal EMG/Stimulation Sensor
• 00852423006165: Pathway® STM-10
• 00852423006141: Pathway® TR-20 Dual Channel EMG Trainer