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K-ASSAY® Ferritin Calibrator

FDA UDI

Class II (US FDA UDI)

by Kamiya Biomedical Company, Llc

Identity

Trade Name
K-ASSAY® Ferritin Calibrator FDA UDI
Generic Name
Ferritin IVD, calibrator FDA UDI
Device Name
For the calibration of the K-ASSAY® Ferritin assay. FDA UDI
Model / Reference
KAI-094C FDA UDI
Description
For the calibration of the K-ASSAY® Ferritin assay. FDA UDI

Identifiers

Catalog Number
KAI-094C FDA UDI
Primary DI / UDI-DI
00816426020689 FDA UDI
510(k) Number
K050944 FDA UDI
FDA Product Code
JIT FDA UDI
GMDN Term
Ferritin IVD, calibrator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1150 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

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: Ferritin IVD, calibrator

K-ASSAY® Ferritin Calibrator by Kamiya Biomedical Company, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ferritin IVD, calibrator.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8279b7ee-eea1-4fc3-83b1-72107bcf5a70 37 fields · synced May 30, 2026