Cannula FG2200

GUDID 06938695522009

KMC Kyphoplasty System consists of four components: Balloon Catheter Tool Kit (including Bone Filler Device, Dilator, Cannula, Drill and Guide Wire) P

Shanghai Kinetic Medical Co., Ltd.

Bone access cannula

• Primary Device ID: 06938695522009
• NIH Device Record Key: 83213540-c8be-4634-b28d-70d770bedcaa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cannula
• Version Model Number: FG2200
• Catalog Number: FG2200
• Company DUNS: 528198569
• Company Name: Shanghai Kinetic Medical Co., Ltd.
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +862150720558
• Email: qingmeiwei@kineticmedinc.com

Operating and Storage Conditions

• Storage Environment Humidity: Between 0 Percent (%) Relative Humidity and 80 Percent (%) Relative Humidity
• Storage Environment Temperature: Between 18 Degrees Celsius and 25 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	06938695522009 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K113742

FDA Product Code

• HRX: Arthroscope

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: 2016-12-05

On-Brand Devices [Cannula]

• 06938695522009: KMC Kyphoplasty System consists of four components: Balloon Catheter Tool Kit (including Bone Fi
• 06938695537669: FG2210