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Dentocore Body

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref DABODY1-10

by Itena Clinical

Identity

Trade Name
DENTOCORE BODY EUDAMEDFDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
Core build-up Cementation Composite EUDAMED
Model / Reference
DABODY1-10 EUDAMED
Automix FDA UDI

Identifiers

Catalog Number
DABODY1-10 FDA UDI
Primary DI / UDI-DI
03760260222013 EUDAMEDFDA UDI
Basic UDI-DI
B-03760260222013 EUDAMED
FDA Product Code
EBF FDA UDI
EMDN Code
Q01010199 DENTAL RESTORATION DEVICES - OTHER EUDAMED
GMDN Term
Dental composite resin FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
872.3690 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

Yes

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Dentocore Body by Itena Clinical — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental composite resin.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Itena Clinical

Sources (2)

  • FDA UDI f90ad94f-f593-4251-9eb0-c7fff636219e 33 fields · synced Jul 12, 2026
  • EUDAMED 7b2eca1a-b43d-463b-a473-a35182b818e4 61 fields · synced Jul 12, 2026