PAPARELLA-TYPE VENT TUBE 1.14MM ID ULTRASIL™ SILICONE

GUDID 00821925026193

Gyrus Acmi, Inc.

Tympanostomy tube

• Primary Device ID: 00821925026193
• NIH Device Record Key: f7ce3d42-7cc4-463e-83fa-1d5f584af45c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PAPARELLA-TYPE VENT TUBE 1.14MM ID ULTRASIL™ SILICONE
• Version Model Number: 70240280
• 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	00821925026193 [Package]; Contains: 00821925032217; Package: [6 Units]; In Commercial Distribution
GS1	00821925032217 [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: 2016-10-03

On-Brand Devices [PAPARELLA-TYPE VENT TUBE 1.14MM ID ULTRASIL™ SILICONE]

• 00821925026209: 70240281
• 00821925026193: 70240280