CO2 Hose and Yoke

GUDID 00817183020196

CO2 Hose and Yoke for use with Laparoscopic insufflators

NORTHGATE TECHNOLOGIES INC.

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• Primary Device ID: 00817183020196
• NIH Device Record Key: 899a1a9a-1b46-414c-964b-dba1570c2548
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CO2 Hose and Yoke
• Version Model Number: 7-510-09
• Company DUNS: 627969264
• Company Name: NORTHGATE TECHNOLOGIES INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817183020196 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K022052

FDA Product Code

• HIF: Insufflator, Laparoscopic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-10-13

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