GUDID 00385640027342

SUMMIT MEDICAL, INC.

Instrument tray

• Primary Device ID: 00385640027342
• NIH Device Record Key: af618de7-4120-4899-bc8a-e83745e546b3
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: OM-1012-AE
• Company DUNS: 965484699
• Company Name: SUMMIT MEDICAL, 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00385640027342 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K051157

FDA Product Code

• KCT: Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-08-09
• Device Publish Date: 2017-03-11

Devices Manufactured by SUMMIT MEDICAL, INC.

• 00385640084796 - INSTRUSAFE: 2025-01-17
• 00385640084802 - INSTRUSAFE: 2025-01-17
• 00385640084789 - INSTRUSAFE: 2025-01-16
• 00385640084765 - INSTRUSAFE: 2025-01-15
• 00385640084772 - INSTRUSAFE: 2025-01-15
• 00385640084758 - INSTRUSAFE: 2025-01-14
• 00385640084741 - INSTRUSAFE: 2025-01-10
• 00385640084734 - INSTRUSAFE: 2025-01-08