← Back to catalogue

Obtura Max Base Unit and Sup

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 823-803

by Young Innovations Inc

Identity

Trade Name
Obtura Max Base Unit and Sup EUDAMED
Obtura Spartan FDA UDI
Generic Name
Endodontic obturation system FDA UDI
Device Name
Obtura Max Base Unit and Sup EUDAMED
Obtura III Max System FDA UDI
Model / Reference
823-803 EUDAMEDFDA UDI
Description
Obtura III Max System FDA UDI

Identifiers

Catalog Number
823-803 FDA UDI
Primary DI / UDI-DI
10843471100414 EUDAMED
00843471100417 FDA UDI
Basic UDI-DI
B-10843471100414 EUDAMED
FDA Product Code
EKR FDA UDI
EMDN Code
Q01010199 DENTAL RESTORATION DEVICES - OTHER EUDAMED
GMDN Term
Endodontic obturation system FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Endocrine Disruptor

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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental appliance fabrication material, ceramic

Obtura Max Base Unit and Sup by Young Innovations, Inc. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, ceramic.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
US-MF-000017796
Authorised Representative
Young Microbrush Ireland Ltd IE-AR-000011249

Sources (2)

  • EUDAMED 49dc4120-b096-429e-bc74-b84dda1b5a48 61 fields · synced Jun 18, 2026
  • FDA UDI 214a6465-bbe1-4227-a7c4-c3d7062ed02a 35 fields · synced May 30, 2026