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DRI™ Fentanyl II Negative Calibrator

FDA UDI

Class II (US FDA UDI)

by Ark Diagnostics Inc

Identity

Trade Name
DRI™ Fentanyl II Negative Calibrator FDA UDI
Generic Name
Opiate/opiate metabolite IVD, calibrator FDA UDI
Device Name
DRI™ Fentanyl II Negative Calibrator (Thermo Fisher) is intended for use in the calibration of the DRI™ Fentanyl II Assay. FDA UDI
Model / Reference
10028874 FDA UDI
Description
DRI™ Fentanyl II Negative Calibrator (Thermo Fisher) is intended for use in the calibration of the DRI™ Fentanyl II Assay. FDA UDI

Identifiers

Catalog Number
10028874 FDA UDI
Primary DI / UDI-DI
00812101030776 FDA UDI
FDA Product Code
DLJ FDA UDI
GMDN Term
Opiate/opiate metabolite IVD, calibrator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3200 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Opiate/opiate metabolite IVD, calibrator

DRI™ Fentanyl II Negative Calibrator by Ark Diagnostics Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Opiate/opiate metabolite IVD, calibrator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ark Diagnostics Inc

Sources (1)

  • FDA UDI 83ebc369-fd44-442d-9e95-7afda1170605 36 fields · synced May 30, 2026