MADSEN Capella2 DP

GUDID 00817020029900

INTELLIGENT HEARING SYSTEMS CORP.

Otoacoustic emission system, line-powered Otoacoustic emission system, line-powered Otoacoustic emission system, line-powered

• Primary Device ID: 00817020029900
• NIH Device Record Key: e8d5de36-c219-46f6-b556-c21969f29847
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MADSEN Capella2 DP
• Version Model Number: M016000A
• Company DUNS: 154870455
• Company Name: INTELLIGENT HEARING SYSTEMS CORP.
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817020029900 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K061443

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: 2018-07-06
• Device Publish Date: 2016-09-24

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