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QuinGas

FDA UDI

Class I (US FDA UDI)

by Quintron Instrument Co. Inc.

Identity

Trade Name
QuinGas FDA UDI
Generic Name
Calibration gas/non-refillable cylinder FDA UDI
Device Name
QUINGAS, BREATHTRACKER CALIBRATION FDA UDI
Model / Reference
QT07500-G FDA UDI
Description
QUINGAS, BREATHTRACKER CALIBRATION FDA UDI

Identifiers

Catalog Number
QT07500-G FDA UDI
Primary DI / UDI-DI
00850010197326 FDA UDI
FDA Product Code
BXK FDA UDI
GMDN Term
Calibration gas/non-refillable cylinder FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Calibration gas/non-refillable cylinder

QuinGas by Quintron Instrument Co. Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Calibration gas/non-refillable cylinder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6f688021-ad0c-43fb-a951-acd17e7c5987 34 fields · synced May 29, 2026