Patient Sample Drying Tube QT01135-K

GUDID 00850010197227

DRYING TUBE, PATIENT SAMPLE

QUINTRON INSTRUMENT COMPANY, INC.

Gas chromatography analyser IVD

• Primary Device ID: 00850010197227
• NIH Device Record Key: 68332606-d6e5-4a7b-8311-7681878f34a6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Patient Sample Drying Tube
• Version Model Number: QT01135-K
• Catalog Number: QT01135-K
• Company DUNS: 874498744
• Company Name: QUINTRON INSTRUMENT COMPANY, INC.
• Device Count: 1
• DM Exempt: true
• 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	00850010197227 [Primary]

FDA Product Code

• NRH: System, Breath Measurement

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: 2023-03-23
• Device Publish Date: 2023-03-15

Devices Manufactured by QUINTRON INSTRUMENT COMPANY, INC.

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• 00850010197937 - LOANER ALVEOVAC EXTRACTOR: 2023-03-27
• 00850010197944 - EXTRACTOR REPAIR: 2023-03-27
• 00850010197920 - EASYSAMPLER ASM, 793275: 2023-03-24
• 00850010197906 - BT GC LOANER SC: 2023-03-24
• 00850010197913 - BREATHTRACKER SERIES REPAIR: 2023-03-24
• 00850010197005 - AlveoSampler: 2023-03-23 KIT, ALVEOSAMPLER ONLY, NO SUBSTRATE
• 00850010197012 - GaSampler Bag, Single-Patient: 2023-03-23 BAG, COLLECTION, GASAMPLER, SINGLE PATIENT