QMC1771E

GUDID 00724995190651

The Quick Connect for Intuitive Surgical Ion Fully Articulating Catheter and Peripheral Vision Probe used with the C1220E Directed Flow Processing Container and Tray when used in the SYSTEM 1E and SYSTEM 1 endo Liquid Chemical Sterilant Processing Systems.

Corporation Steris Canada

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• Primary Device ID: 00724995190651
• NIH Device Record Key: b8f3fa52-860d-4a19-8f0a-c55958a2409e
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: QMC1771E
• Catalog Number: QMC1771E
• Company DUNS: 202659140
• Company Name: Corporation Steris Canada
• 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: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

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Device Identifiers

Device Issuing Agency	Device ID
GS1	00724995190651 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K090036

FDA Product Code

• MED: Sterilant, medical devices

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-06-12
• Device Publish Date: 2020-06-04

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