PAPARELLA VENT TUBE WITHOUT TAB 1.02MM ID ULTRASIL™ SILICONE

GUDID 00821925021655

Gyrus Acmi, Inc.

Tympanostomy tube

• Primary Device ID: 00821925021655
• NIH Device Record Key: 5861c4df-fcda-4813-9958-2b899f6bcab8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PAPARELLA VENT TUBE WITHOUT TAB 1.02MM ID ULTRASIL™ SILICONE
• Version Model Number: 70921773
• Company DUNS: 007198742
• Company Name: Gyrus Acmi, Inc.
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00821925021655 [Package]; Contains: 00821925032934; Package: [30 Units]; In Commercial Distribution
GS1	00821925032934 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K960477

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: 2016-10-06

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