CoPilot VL Disposable Sheaths, Size 2 Case of 10 3720

GUDID 01810049840029

Dilon Technologies, Inc.

Video intubation laryngoscope kit

• Primary Device ID: 01810049840029
• NIH Device Record Key: 295c41d8-30fb-416a-bc51-b8422b943b74
• Commercial Distribution Discontinuation: 2022-12-08
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: CoPilot VL Disposable Sheaths, Size 2 Case of 10
• Version Model Number: 3720
• Catalog Number: 3720
• Company DUNS: 061727272
• Company Name: Dilon Technologies, Inc.
• Device Count: 10
• 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: 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	01810049840029 [Unit of Use]
GS1	10810049840027 [Primary]

FDA Product Code

• CCW: Laryngoscope, Rigid

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2023-02-20
• Device Publish Date: 2022-12-08

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• 00810049840051 - Navigator Standard Lymphactic Mapping Probe, 14mm, Wired, Angled: 2023-02-20
• 00810049840068 - Navigator Standard Lymphactic Mapping Probe, 14mm, Wired, Straight: 2023-02-20
• 00810049840075 - Navigator Wireless Probe, 14mm Angled: 2023-02-20
• 00810049840082 - Navigator Wireless Probe, 14mm Straight: 2023-02-20