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Resin Teeth / DCL / PE

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 608240

by Ivoclar Vivadent Aktiengesellschaft

Identity

Trade Name
SR Vivodent Plus DCL Juego de 6 SP13 B4 EUDAMED
Resin Teeth / DCL / PE FDA UDI
Generic Name
Resin artificial teeth FDA UDI
Device Name
Ivostar / Gnathostar, Ivocryl, Resin Teeth / DCL / PE, Resin Teeth S PE / S DCL, SR Phonares II EUDAMED
SR Vivodent Plus DCL Set of 6 UP13 B4 FDA UDI
Model / Reference
608240 EUDAMEDFDA UDI
Description
SR Vivodent Plus DCL Set of 6 UP13 B4 FDA UDI

Identifiers

Catalog Number
608240 FDA UDI
Primary DI / UDI-DI
07615208373639 EUDAMEDFDA UDI
Basic UDI-DI
76152082APROS004VZ EUDAMED
FDA Product Code
ELM FDA UDI
EMDN Code
Q010699 MATERIALS FOR THE PREPARATION OF CUSTOM-MADE DENTAL DEVICES - OTHER EUDAMED
GMDN Term
Resin artificial teeth FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
872.3590 FDA UDI
Market of Registration
Liechtenstein EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Resin artificial teeth

Resin Teeth / DCL / PE by Ivoclar Vivadent Aktiengesellschaft — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Resin artificial teeth.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 1b99fd22-b897-470c-84d5-4a8239074c08 34 fields · synced Aug 3, 2026
  • EUDAMED 0833e859-5d89-497c-8ad1-046e1f9da146 61 fields · synced Aug 3, 2026