NITRONOX INHALATION HOSPITAL MIXER ANALGESIA MACHINE

GUDID 00816711020370

NITRONOX INHALATION ANALGESIA

PARKER-HANNIFIN CORPORATION

Inhalational analgesia unit

• Primary Device ID: 00816711020370
• NIH Device Record Key: 494ec07f-76e6-498c-a75f-0f106f4be3bb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NITRONOX INHALATION HOSPITAL MIXER ANALGESIA MACHINE
• Version Model Number: NOX-5000H
• 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	00816711020370 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K760766

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: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-24

On-Brand Devices [NITRONOX INHALATION HOSPITAL MIXER ANALGESIA MACHINE]

• 00816711020387: NITRONOX,HOSPITAL W/DEM VALVE
• 00816711020370: NITRONOX INHALATION ANALGESIA