TY-MA Set

GUDID 04260223143717

Set consisting of: (TY-MA, ear tips, probe tips, cavity)

PATH medical GmbH

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• Primary Device ID: 04260223143717
• NIH Device Record Key: f081de82-2254-49c5-a4f7-045b3957010a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TY-MA Set
• Version Model Number: 100947-N-SET
• Company DUNS: 551540334
• Company Name: PATH medical GmbH
• 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: true
• 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	04260223143717 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K133012

FDA Product Code

• ETY: Tester, Auditory Impedance

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: 2022-01-25
• Device Publish Date: 2022-01-17

On-Brand Devices [TY-MA Set ]

• 04260223143618: Set consisting of: (TY-MA, ear tips, probe tips, cavity)
• 04260223143717: Set consisting of: (TY-MA, ear tips, probe tips, cavity)