SURGICAL ASPIRATOR TIPS

GUDID D89260705530902

MAXILL, INC.

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• Primary Device ID: D89260705530902
• NIH Device Record Key: 1f00dec0-a9d9-47a9-99f2-4553d0e74da5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SURGICAL ASPIRATOR TIPS
• Version Model Number: 6070553090
• Company DUNS: 079343581
• Company Name: MAXILL, INC.
• Device Count: 25
• 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: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D89260705530900 [Unit of Use]
HIBCC	D89260705530901 [Primary]
HIBCC	D89260705530902 [Package]; Contains: D89260705530901; Package: Case [500 Units]; In Commercial Distribution

FDA Product Code

• DYN: Mouthpiece, Saliva Ejector

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: 2022-10-28
• Device Publish Date: 2022-10-20

On-Brand Devices [SURGICAL ASPIRATOR TIPS]

• D89260705530912: 6070553091
• D89260705530902: 6070553090