MXR FLOWMETER

GUDID 00816711020059

MXR FLOW METER WITH BAG TEE

PARKER-HANNIFIN CORPORATION

Inhalational analgesia unit

• Primary Device ID: 00816711020059
• NIH Device Record Key: 7a7377c5-9be8-4ee5-af1e-6673b9350ba6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MXR FLOWMETER
• Version Model Number: 3000
• Company DUNS: 004175550
• Company Name: PARKER-HANNIFIN CORPORATION
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816711020059 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K923781

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: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-24

Devices Manufactured by PARKER-HANNIFIN CORPORATION

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• 00816711024279 - MIDAS, REMOTE, 50%-W-O2: 2024-10-22 Midas Flowmeter, Remote, 50% Max, O2 Control
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