COMO White

GUDID 08800019110729

B& L Biotech, inc.

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• Primary Device ID: 08800019110729
• NIH Device Record Key: 522a3a2a-97de-485a-a375-c4a951430492
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: COMO White
• Version Model Number: COMW
• Company DUNS: 687338285
• Company Name: B& L Biotech, 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800019110729 [Primary]

FDA Product Code

• KXR: Applicator, Resin

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: 2023-06-23
• Device Publish Date: 2023-06-15

Devices Manufactured by B& L Biotech, inc.

• 08800019110651 - POMO Black: 2023-06-23
• 08800019110668 - POMO White: 2023-06-23
• 08800019110675 - POMO Pink: 2023-06-23
• 08800019110712 - COMO Black: 2023-06-23
• 08800019110729 - COMO White: 2023-06-23
• 08800019110729 - COMO White: 2023-06-23
• 08800019110736 - COMO Pink: 2023-06-23
• 08800019110743 - COMO Tip: 2023-06-23
• 08800019110750 - COMO Tip: 2023-06-23