← Back to catalogue

Nova

FDA UDI

Class I (US FDA UDI)

by Nova Biomedical Corporation

Identity

Trade Name
Nova FDA UDI
Generic Name
Multiple clinical chemistry analyte monitoring system IVD, point-of-care FDA UDI
Device Name
Syringe Clot Catcher FDA UDI
Model / Reference
Nova FDA UDI
Description
Syringe Clot Catcher FDA UDI

Identifiers

Catalog Number
38883 FDA UDI
Primary DI / UDI-DI
00385480388832 FDA UDI
FDA Product Code
LXG FDA UDI
GMDN Term
Multiple clinical chemistry analyte monitoring system IVD, point-of-care FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Multiple clinical chemistry analyte monitoring system IVD, point-of-care

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

Similar devices

Also classified as Multiple clinical chemistry analyte monitoring system IVD, point-of-care.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Nova Biomedical Corporation

Sources (1)

  • FDA UDI ffed8bdf-e12d-463b-a16c-434ba623d590 35 fields · synced Jun 6, 2026