GUDID 00385640001724

SUMMIT MEDICAL, INC.

Tympanostomy tube

• Primary Device ID: 00385640001724
• NIH Device Record Key: 8906b09c-4ac0-49da-99a5-cb1cfb4f1189
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: VT-0903-01
• Company DUNS: 965484699
• Company Name: SUMMIT MEDICAL, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00385640001724 [Primary]
GS1	10385640001721 [Package]; Package: Box [6 Units]; In Commercial Distribution
GS1	20385640001728 [Package]; Package: Box [50 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K830228

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: 2016-09-12

Devices Manufactured by SUMMIT MEDICAL, INC.

• 00385640088022 - INSTRUSAFE: 2025-08-22
• 00385640088039 - INSTRUSAFE: 2025-08-22
• 00385640087971 - INSTRUSAFE: 2025-08-21
• 00385640087988 - INSTRUSAFE: 2025-08-21
• 00385640087995 - INSTRUSAFE: 2025-08-21
• 00385640088008 - INSTRUSAFE: 2025-08-21
• 00385640088015 - INSTRUSAFE: 2025-08-21
• 00385640087957 - INSTRUSAFE: 2025-08-20