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NovaPro

FDA UDI

Class II (US FDA UDI)

by Nanova Biomaterials Inc

Identity

Trade Name
NovaPro FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
NovaPro Sample Kit 1 A2 Flow Syringe & 3 A2 Fill Carpules FDA UDI
Model / Reference
141611 FDA UDI
Description
NovaPro Sample Kit 1 A2 Flow Syringe & 3 A2 Fill Carpules FDA UDI

Identifiers

Catalog Number
141611 FDA UDI
Primary DI / UDI-DI
00816537020851 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Dental composite resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3690 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: Dental composite resin

NovaPro by Nanova Biomaterials Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental composite resin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fadf69e1-d03c-4b2f-b4e8-36612aa4fa48 35 fields · synced Jun 1, 2026