QuinGas QT07500-G

GUDID 00850010197326

QUINGAS, BREATHTRACKER CALIBRATION

QUINTRON INSTRUMENT COMPANY, INC.

Calibration gas/non-refillable cylinder

• Primary Device ID: 00850010197326
• NIH Device Record Key: 6f688021-ad0c-43fb-a951-acd17e7c5987
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: QuinGas
• Version Model Number: QT07500-G
• Catalog Number: QT07500-G
• Company DUNS: 874498744
• Company Name: QUINTRON INSTRUMENT COMPANY, INC.
• 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: true
• 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	00850010197326 [Primary]

FDA Product Code

• BXK: Gas, Calibration (Specified Concentration)

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: 2022-05-30
• Device Publish Date: 2022-05-20

On-Brand Devices [QuinGas]

• 00850010197326: QUINGAS, BREATHTRACKER CALIBRATION
• 00850010197319: QUINGAS, MICROLYZER CALIBRATION