BlenderBuddy R219P20-007

GUDID 00817770025634

BlenderBuddy for Precision Medical MicroMax with 0-5 LPM and 0-200cc Thorpe Flowmeters

MAXTEC, LLC

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• Primary Device ID: 00817770025634
• NIH Device Record Key: 4b829b77-9d70-4820-8715-888a52137b7e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BlenderBuddy
• Version Model Number: BlenderBuddy
• Catalog Number: R219P20-007
• Company DUNS: 169911828
• Company Name: MAXTEC, LLC
• 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: true
• Serial Number: false
• Manufacturing Date: true
• 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	00817770025634 [Primary]

FDA Product Code

• CAX: Flowmeter, Tube, Thorpe, Back-Pressure Compensated

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: 2021-11-02
• Device Publish Date: 2021-10-25

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