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Nova Max

FDA UDI

Class I (US FDA UDI)

by Nova Biomedical Corporation

Identity

Trade Name
NOVA MAX FDA UDI
Generic Name
Multiple blood gas/haemoximetry/electrolyte analyte IVD, control FDA UDI
Device Name
Nova Max Plus Glu/Ket Control Solution - Mid FDA UDI
Model / Reference
Plus FDA UDI
Description
Nova Max Plus Glu/Ket Control Solution - Mid FDA UDI

Identifiers

Catalog Number
49640 FDA UDI
Primary DI / UDI-DI
00385480496407 FDA UDI
510(k) Number
K101633 FDA UDI
FDA Product Code
JJY FDA UDI
GMDN Term
Multiple blood gas/haemoximetry/electrolyte analyte IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 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

Yes

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: Multiple blood gas/haemoximetry/electrolyte analyte IVD, control

Nova Max by Nova Biomedical Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple blood gas/haemoximetry/electrolyte analyte IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7b03d5f9-9688-4e45-8237-37083e441b44 37 fields · synced Jun 8, 2026