Phonak 050-0907-G1

GUDID 07612847819160

Phonak Ambra SP (mid cloud gray)

Phonak AG

Behind-the-ear air-conduction hearing aid

• Primary Device ID: 07612847819160
• NIH Device Record Key: a8f22e12-8409-4afa-806d-d10e119b4426
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Phonak
• Version Model Number: 050-0907-G1
• Catalog Number: 050-0907-G1
• Company DUNS: 480089517
• Company Name: Phonak AG
• Device Count: 1
• DM Exempt: true
• 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

Customer Support Contacts

• Phone: +41589280101
• Email: contact@phonak.com
• Phone: +41589280101
• Email: contact@phonak.com
• Phone: +41589280101
• Email: contact@phonak.com
• Phone: +41589280101
• Email: contact@phonak.com
• Phone: +41589280101
• Email: contact@phonak.com
• Phone: +41589280101
• Email: contact@phonak.com
• Phone: +41589280101
• Email: contact@phonak.com
• Phone: +41589280101
• Email: contact@phonak.com
• Phone: +41589280101
• Email: contact@phonak.com
• Phone: +41589280101
• Email: contact@phonak.com
• Phone: +41589280101
• Email: contact@phonak.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07612847819160 [Primary]

FDA Product Code

• OSM: Hearing aid, air conduction with wireless technology

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-12

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• 07613275472552: Lyric3 (XXL)
• 07613275472545: Lyric3 (XL)
• 07613275471890: Lyric3 (L)
• 07613275471883: Lyric3 (M)
• 07613275471876: Lyric3 (S)