Phonak Terra BTE-SP 050-1101-P3

GUDID 07613389665260

Sonova AG

Air-conduction hearing aid, behind-the-ear

• Primary Device ID: 07613389665260
• NIH Device Record Key: 85e1f744-b622-44d6-88cf-2c04c3b1409c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Phonak Terra BTE-SP
• Version Model Number: (sandalwood)
• Catalog Number: 050-1101-P3
• 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	07613389665260 [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: 2023-11-30
• Device Publish Date: 2023-11-22

On-Brand Devices [Phonak Terra BTE-SP ]

• 07613389665277: (silver gray)
• 07613389665260: (sandalwood)
• 07613389663204: (beige)
• 07613389867848: (velvet black)