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T-Connector, Plastic

FDA UDI

Class I (US FDA UDI)

by Quintron Instrument Co. Inc.

Identity

Trade Name
T-CONNECTOR, PLASTIC FDA UDI
Generic Name
Breath specimen container IVD FDA UDI
Model / Reference
QT00850-P FDA UDI

Identifiers

Catalog Number
QT00850-P FDA UDI
Primary DI / UDI-DI
00850010197036 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Breath specimen container IVD

T-Connector, Plastic 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

Manufacturer
Quintron Instrument Co. Inc.

Sources (1)

  • FDA UDI f3d16da1-74be-408f-afd0-625e208f0b63 33 fields · synced Jun 8, 2026