Aqustic

GUDID 00196852460601

HEARING AID

PS Hearing Products Inc

Air-conduction hearing aid, wearable case

• Primary Device ID: 00196852460601
• NIH Device Record Key: 3b851eb8-a0a4-4661-af05-c9d122b1a4aa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Aqustic
• Version Model Number: PHSA-0001-00-00
• Company DUNS: 203273990
• Company Name: PS Hearing Products 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: false
• Serial Number: false
• Manufacturing Date: false
• 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: 519-886-0899
• Email: NICK@ACRPLTD.COM
• Phone: 519-886-0899
• Email: NICK@ACRPLTD.COM
• Phone: 519-886-0899
• Email: NICK@ACRPLTD.COM
• Phone: 519-886-0899
• Email: NICK@ACRPLTD.COM
• Phone: 519-886-0899
• Email: NICK@ACRPLTD.COM
• Phone: 519-886-0899
• Email: NICK@ACRPLTD.COM
• Phone: 519-886-0899
• Email: NICK@ACRPLTD.COM
• Phone: 519-886-0899
• Email: NICK@ACRPLTD.COM
• Phone: 519-886-0899
• Email: NICK@ACRPLTD.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00196852460601 [Primary]

FDA Product Code

• ESD: Hearing Aid, Air Conduction

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: 2022-08-02
• Device Publish Date: 2022-07-25