Phonak Audéo I90-Sphere 050-1029-P8B3

GUDID 07613389753226

Sonova AG

Air-conduction hearing aid, receiver-in-canal

• Primary Device ID: 07613389753226
• NIH Device Record Key: deb63bdf-ac43-4400-a75f-b5944fe62fab
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Phonak Audéo I90-Sphere
• Version Model Number: (velvet black)
• Catalog Number: 050-1029-P8B3
• Company DUNS: 480662550
• Company Name: Sonova AG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Unsafe
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613389753226 [Primary]

FDA Product Code

• KLW: Masker, Tinnitus

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: 2024-07-08
• Device Publish Date: 2024-06-28

On-Brand Devices [Phonak Audéo I90-Sphere ]

• 07613389699104: (atlantic green)
• 07613389699098: (sienna red)
• 07613389699081: (copper)
• 07613389686647: (velvet black)
• 07613389686630: (graphite gray)
• 07613389686623: (champagne)
• 07613389686616: (chestnut)
• 07613389686609: (sandalwood)
• 07613389686593: (sand beige)
• 07613389686586: (beige)
• 07613389583021: (silver gray)
• 07613389753134: (sienna red)
• 07613389753127: (copper)
• 07613389753226: (velvet black)
• 07613389753219: (graphite gray)
• 07613389753202: (silver gray)
• 07613389753196: (champagne)
• 07613389753189: (chestnut)
• 07613389753172: (sandalwood)
• 07613389753165: (sand beige)
• 07613389753158: (beige)
• 07613389753141: (atlantic green)