MaxFlo2

GUDID 00853061006135

Low Flow with MaxO2+ DISS Fitting Kit

MAXTEC, LLC

Oxygen/air breathing gas mixer, hospital

• Primary Device ID: 00853061006135
• NIH Device Record Key: d84ea97c-9b1a-4e11-9c6a-2a78c64b6ce1
• Commercial Distribution Discontinuation: 2019-05-06
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: MaxFlo2
• Version Model Number: R223P01-005
• Company DUNS: 169911828
• Company Name: MAXTEC, LLC
• 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: false
• Lot Batch: false
• Serial Number: true
• 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	00853061006135 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K113232

FDA Product Code

• BZR: Mixer, Breathing Gases, Anesthesia Inhalation

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: 2019-05-07
• Device Publish Date: 2019-01-14

On-Brand Devices [MaxFlo2]

• 00817770020806: MaxFlo2 Mini 0-70 LPM
• 00817770020790: High Flow System
• 00817770020783: Low Flow System
• 00853061006159: High Flow Spanish Labeled
• 00853061006142: High Flow with MaxO2+ Nist Fitting Kit
• 00853061006135: Low Flow with MaxO2+ DISS Fitting Kit
• 00853061006067: High Flow with MaxO2+, DISS Fitting Kit
• 00853061006050: Low low with MaxO2+A, DISS Fitting Kit
• 00853061006036: High Flow with NIST Fitting
• 00853061006029: MaxFlo2 High Flow with DISS Fitting
• 00853061006005: MaxFlo2 Low Flow DISS Fitting