Maico

GUDID 08584270045074

Diagnostic Group LLC

Otoacoustic emission system, battery-powered

• Primary Device ID: 08584270045074
• NIH Device Record Key: 342fb2f5-e0cf-4cce-8ee9-88b902a99da2
• Commercial Distribution Discontinuation: 2020-05-26
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Maico
• Version Model Number: EroScan
• Company DUNS: 175799717
• Company Name: Diagnostic Group LLC
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	08584270045074 [Primary]

FDA Product Code

• EWO: Audiometer

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2024-11-04
• Device Publish Date: 2018-07-24

On-Brand Devices [Maico]

• 08584270041557: MA 41
• 08584270041533: MA 25
• 08584270041526: MA 1
• 08584270041298: Digital Pilot Test
• 08584270041267: MA 27
• 08584270041168: MA 52
• 08584270041151: MA 42
• 08584270045074: EroScan