Arc tubing connection 231100

GUDID E2392311001

No.

Dreve Otoplastik GmbH

Air-conduction hearing aid acoustic tube

• Primary Device ID: E2392311001
• NIH Device Record Key: 7f9ee235-210e-412c-94a2-9d1c148287f1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Arc tubing connection
• Version Model Number: 231100
• Catalog Number: 231100
• Company DUNS: 315808340
• Company Name: Dreve Otoplastik GmbH
• 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: true
• 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

Customer Support Contacts

• Phone: +49230388070
• Email: otoplastik@dreve.de

Operating and Storage Conditions

• Storage Environment Temperature: Between 18 Degrees Celsius and 28 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	E2392311001 [Primary]

FDA Product Code

• ESD: Hearing Aid, Air-Conduction, 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: 2023-01-12
• Device Publish Date: 2023-01-04

On-Brand Devices [Arc tubing connection]

• E2392391: No.
• E239231101: No.
• E2392311001: No.
• E2392041101: No.
• E23920411001: No.