GUDID 10814716020859

Smoke Evacuation Tubing

COASTAL LIFE TECHNOLOGIES, INC.

Surgical plume evacuation system tube Surgical plume evacuation system tube Surgical plume evacuation system tube Surgical plume evacuation system tube Surgical plume evacuation system tube Surgical plume evacuation system tube Surgical plume evacuation system tube Surgical plume evacuation system tube Surgical plume evacuation system tube Surgical plume evacuation system tube Surgical plume evacuation system tube Surgical plume evacuation system tube Surgical plume evacuation system tube

• Primary Device ID: 10814716020859
• NIH Device Record Key: d6157057-2ac9-4517-9b4c-e784497c2fcb
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 300-842
• Company DUNS: 809254670
• Company Name: COASTAL LIFE TECHNOLOGIES, 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00814716020852 [Primary]
GS1	10814716020859 [Package]; Contains: 00814716020852; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• FCZ: Tube, Smoke Removal, Endoscopic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-23

Devices Manufactured by COASTAL LIFE TECHNOLOGIES, INC.

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