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Nova Primary

FDA UDI

Class II (US FDA UDI)

by Nova Biomedical Corporation

Identity

Trade Name
Nova Primary FDA UDI
Generic Name
Glucose IVD, calibrator FDA UDI
Device Name
Nova Primary Calibrator Cartridge 150 Sample FDA UDI
Model / Reference
Nova Primary Calibrator Cartridge 150 Sample FDA UDI
Description
Nova Primary Calibrator Cartridge 150 Sample FDA UDI

Identifiers

Catalog Number
63167 FDA UDI
Primary DI / UDI-DI
00385480631679 FDA UDI
510(k) Number
K203549 FDA UDI
FDA Product Code
CGA FDA UDI
GMDN Term
Glucose IVD, calibrator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1345 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Glucose IVD, calibrator

Nova Primary by Nova Biomedical Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glucose 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 885a1a58-9baa-4a22-b2ab-7d492c0de0e2 37 fields · synced Jun 8, 2026