SafeView 5801.4601

GUDID 00850022178764

KINOS MEDICAL INC

Arthroscopic access cannula, single-use

• Primary Device ID: 00850022178764
• NIH Device Record Key: a0a53e77-5c76-4333-96b0-a05145f67fb4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SafeView
• Version Model Number: 5801.4601
• Catalog Number: 5801.4601
• Company DUNS: 081112239
• Company Name: KINOS MEDICAL INC
• Device Count: 1
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850022178764 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

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: 2020-10-20
• Device Publish Date: 2020-10-12

On-Brand Devices [SafeView]

• 00850022178771: 5801.4602
• 00850022178764: 5801.4601