COLLAR BUTTON VENT TUBE 127MM ID 15MM IF BLUE FLUOROPLASTIC

GUDID 00821925033979

Ventilate the middle ear subsequent to otitis media Elimiate fluid buildup in the middle ear while creating an avenue passage for air pressure equalization on either side of the drum.

Gyrus Acmi, Inc.

Tympanostomy tube

• Primary Device ID: 00821925033979
• NIH Device Record Key: 85534b04-ba49-4f64-bcb7-c2cf8ad363e4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: COLLAR BUTTON VENT TUBE 127MM ID 15MM IF BLUE FLUOROPLASTIC
• Version Model Number: 70145060
• Company DUNS: 007198742
• Company Name: Gyrus Acmi, Inc.
• Device Count: 2
• 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: true
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
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• Phone: 18002623540
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• Phone: 18002623540
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• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
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• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
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• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
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• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
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• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx
• Phone: 18002623540
• Email: xxx@xxx.xxx

Device Identifiers

Device Issuing Agency	Device ID
GS1	00821925020344 [Package]; Package: [60 Units]; In Commercial Distribution
GS1	00821925033979 [Primary]
GS1	00821925040724 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K992222

FDA Product Code

• ETD: Tube, Tympanostomy

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-10-24

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