Olive Plus

GUDID 88000346000762

Olive Union inc

Air-conduction hearing aid, receiver-in-canal

• Primary Device ID: 88000346000762
• NIH Device Record Key: 481e536b-3f0d-4c42-83f6-be83147692ac
• Commercial Distribution Discontinuation: 2023-04-11
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Olive Plus
• Version Model Number: OSE300M
• Company DUNS: 694767953
• Company Name: Olive Union inc
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	88000346000762 [Primary]

FDA Product Code

• QUG: Hearing Aid, Air-Conduction With Wireless Technology, Over The Counter

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: 2023-04-19
• Device Publish Date: 2023-04-11

On-Brand Devices [Olive Plus]

• 88000346001066: OSE300
• 88000346000762: OSE300M
• 08800034600106: OSE300
• 08800034600076: OSE300M