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EasySampler, , Proficiency Test Kit

FDA UDI

Class I (US FDA UDI)

by Quintron Instrument Co. Inc.

Identity

Trade Name
EasySampler,, Proficiency Test Kit FDA UDI
Generic Name
Breath specimen container IVD FDA UDI
Device Name
KIT, ANALYTICAL PROFICIENCY TEST, 4T FDA UDI
Model / Reference
QT04202 FDA UDI
Description
KIT, ANALYTICAL PROFICIENCY TEST, 4T FDA UDI

Identifiers

Catalog Number
QT04202 FDA UDI
Primary DI / UDI-DI
00850010197289 FDA UDI
FDA Product Code
NNI FDA UDI
GMDN Term
Breath specimen container IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3250 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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: Breath specimen container IVD

EasySampler, , Proficiency Test Kit by Quintron Instrument Co. Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Breath specimen container IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 856e8a2a-4ede-4577-af5e-4aea8f2b903d 34 fields · synced Jun 8, 2026