Phonak Terra+ BTE-SP 050-1105-P8

GUDID 07613389867886

Sonova AG

Air-conduction hearing aid, behind-the-ear

• Primary Device ID: 07613389867886
• NIH Device Record Key: 7a6ed723-6fd6-40bf-978c-88894d6b25c1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Phonak Terra+ BTE-SP
• Version Model Number: (velvet black)
• Catalog Number: 050-1105-P8
• 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	07613389867886 [Primary]

FDA Product Code

• OSM: Hearing Aid, Air-Conduction With Wireless Technology, Prescription

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: 2025-11-26
• Device Publish Date: 2025-11-18

On-Brand Devices [Phonak Terra+ BTE-SP ]

• 07613389665376: (silver gray)
• 07613389665369: (sandalwood)
• 07613389665352: (sand beige)
• 07613389663549: (beige)
• 07613389867886: (velvet black)