Chinook Suture/Syringe Module

GUDID 00856767008021

Chinook Medical Gear

Suture kit, non-medicated Suture kit, non-medicated Suture kit, non-medicated Suture kit, non-medicated Suture kit, non-medicated Suture kit, non-medicated Suture kit, non-medicated Suture kit, non-medicated Suture kit, non-medicated Suture kit, non-medicated Suture kit, non-medicated Suture kit, non-medicated Suture kit, non-medicated Suture kit, non-medicated Suture kit, non-medicated Suture kit, non-medicated Suture kit, non-medicated Suture kit, non-medicated Suture kit, non-medicated

• Primary Device ID: 00856767008021
• NIH Device Record Key: 4b25405c-7d29-4fe3-85c5-0a250702560c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Chinook Suture/Syringe Module
• Version Model Number: 1210
• Company DUNS: 621904622
• Company Name: Chinook Medical Gear
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00856767008021 [Primary]

FDA Product Code

• OVN: Suture Kit

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: 2018-06-15
• Device Publish Date: 2018-05-15

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