XLP - CPRotector® Deluxe - Orange Nylon Pouch K203-006

GUDID 00766588030067

XLP - CPRotector® Deluxe - Orange Nylon Pouch

Certified Safety Manufacturing, Inc.

Non-rebreathing valve, single-use

• Primary Device ID: 00766588030067
• NIH Device Record Key: 8cf49b72-9752-4565-9914-4c95b55bf79f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: XLP - CPRotector® Deluxe - Orange Nylon Pouch
• Version Model Number: K203-006
• Catalog Number: K203-006
• Company DUNS: 788460483
• Company Name: Certified Safety Manufacturing, Inc.
• 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: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(816)483-9090
• Email: Info@certifiedsafety.com
• Phone: +1(816)483-9090
• Email: Info@certifiedsafety.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00766588030067 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K960587

FDA Product Code

• CBP: Valve, non-rebreathing

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: 2018-12-17
• Device Publish Date: 2018-11-16

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