Summit Hi-Flow Cannula

GUDID 00860003634622

Pristine Surgical LLC

Rigid optical arthroscope, single-use

• Primary Device ID: 00860003634622
• NIH Device Record Key: 5e042200-e4cc-4450-a19d-07c01df1a929
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Summit Hi-Flow Cannula
• Version Model Number: PS-CAN001
• Company DUNS: 080976458
• Company Name: Pristine Surgical LLC
• Device Count: 6
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860003634622 [Unit of Use]
GS1	10860003634629 [Primary]

FDA Product Code

• NBH: Accessories, Arthroscopic

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-09-15
• Device Publish Date: 2025-09-05

Devices Manufactured by Pristine Surgical LLC

• 00860003634622 - Summit Hi-Flow Cannula: 2025-09-15
• 00860003634622 - Summit Hi-Flow Cannula: 2025-09-15
• 00860003634615 - Summit Imagine Processing Unit: 2024-05-28
• 10860003634605 - Summit Single Use Surgical Arthroscope: 2024-05-28