Sanibel Supply

GUDID 05711117223101

Interacoustics A/S

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• Primary Device ID: 05711117223101
• NIH Device Record Key: b8e0db64-ff1b-46bf-9452-082992f9823d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sanibel Supply
• Version Model Number: ADI eartip sample kit, E3
• Company DUNS: 306308354
• Company Name: Interacoustics A/S
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05711117223101 [Primary]

FDA Product Code

• ETT: Cushion, Earphone (For Audiometric Testing)

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: 2023-05-19
• Device Publish Date: 2023-05-11

On-Brand Devices [Sanibel Supply]

• 05711117221848: EARturtle
• 05711117223101: ADI eartip sample kit, E3
• 05711117221107: ADI eartip sample kit, Oaktree
• 05711117208238: ADI eartip sample kit