PHONAK

GUDID EGOL840940

Egger Otoplastik + Labortechnik GmbH

Medical device cleaning/disinfection wipe

• Primary Device ID: EGOL840940
• NIH Device Record Key: 70664634-e1e6-4a46-aec8-316838296160
• Commercial Distribution Discontinuation: 2024-05-26
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: PHONAK
• Version Model Number: C&C Wipe
• Company DUNS: 328465042
• Company Name: Egger Otoplastik + Labortechnik GmbH
• Device Count: 25
• 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: false
• Manufacturing Date: false
• Expiration Date: true
• 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
HIBCC	EGOL840851 [Primary]
HIBCC	EGOL840940 [Unit of Use]

FDA Product Code

• LRJ: Disinfectant, Medical Devices

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: 2024-09-27
• Device Publish Date: 2023-01-01

Devices Manufactured by Egger Otoplastik + Labortechnik GmbH

• EGOL840940 - PHONAK: 2024-09-27
• EGOL840940 - PHONAK: 2024-09-27
• EGOL206001 - egger: 2022-09-08
• EGOL206030 - egger: 2022-09-08
• EGOL206190 - egger: 2022-09-08
• EGOL207001 - egger: 2022-09-08
• EGOL207021 - egger: 2022-09-08
• EGOL207031 - egger: 2022-09-08
• EGOL207041 - egger: 2022-09-08