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Nanoceram-Bright Flow

FDA UDI

Class II (US FDA UDI)

by Dmp Dental Industry S.a.

Identity

Trade Name
NANOCERAM-BRIGHT FLOW FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
Light curing, flowable, nanohybrid composite. Radiopaque, resin-based dental restorative material for anterior and limited posterior restorations. FDA UDI
Model / Reference
A1, 2g FDA UDI
Description
Light curing, flowable, nanohybrid composite. Radiopaque, resin-based dental restorative material for anterior and limited posterior restorations. FDA UDI

Identifiers

Primary DI / UDI-DI
05206569834017 FDA UDI
FDA Product Code
EBC FDA UDI
EBF FDA UDI
GMDN Term
Dental composite resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3765 FDA UDI
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

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

No

FDA UDI

Category: Dental composite resin

Nanoceram-Bright Flow by Dmp Dental Industry S.a. — 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 037434eb-ebeb-4309-b35d-84a4696f00c4 35 fields · synced Jun 8, 2026