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Universal 1

FDA UDI

Class II (US FDA UDI)

by Micerium Spa

Identity

Trade Name
UNIVERSAL 1 FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
CAPO 1 Bulkfill Universal 2g FDA UDI
Model / Reference
CHFFB FDA UDI
Description
CAPO 1 Bulkfill Universal 2g FDA UDI

Identifiers

Catalog Number
CHFFB FDA UDI
Primary DI / UDI-DI
EMICCHFFB0 FDA UDI
510(k) Number
K062906 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

No

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

Yes

FDA UDI

Category: Dental composite resin

Universal 1 by Micerium Spa — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental composite resin.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Micerium Spa

Sources (1)

  • FDA UDI f6bdecab-247c-429a-9a4e-cf0fb18fd875 35 fields · synced Jun 1, 2026