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Quantiferon

FDA UDI

Class I (US FDA UDI)

by Asp Global, LLC

Identity

Trade Name
QUANTIFERON FDA UDI
Generic Name
General specimen receptacle transport container FDA UDI
Device Name
QUANTIFERON REFRIGRATE BAG 1/EA, 100/PK, 1000/CS (10PK/CS) FDA UDI
Model / Reference
504122BC FDA UDI
Description
QUANTIFERON REFRIGRATE BAG 1/EA, 100/PK, 1000/CS (10PK/CS) FDA UDI

Identifiers

Primary DI / UDI-DI
00840216119352 FDA UDI
FDA Product Code
NNK FDA UDI
GMDN Term
General specimen receptacle transport container 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General specimen receptacle transport container

Quantiferon by Asp Global, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General specimen receptacle transport container.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Asp Global, LLC

Sources (1)

  • FDA UDI 27adec9b-fe92-4f79-bcc7-10d83e3ce0b4 33 fields · synced Jun 8, 2026