← Back to catalogue

Variolink Esthetic Try In

FDA UDI

Class II (US FDA UDI)

by Ivoclar Vivadent Aktiengesellschaft

Identity

Trade Name
Variolink Esthetic Try In FDA UDI
Generic Name
Dental cement trial FDA UDI
Device Name
Variolink Esthetic Try. Ref.1.7g warm FDA UDI
Model / Reference
666115WW FDA UDI
Description
Variolink Esthetic Try. Ref.1.7g warm FDA UDI

Identifiers

Catalog Number
666115WW FDA UDI
Primary DI / UDI-DI
DVIV666115WW1 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Dental cement trial 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

Yes

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

Yes

FDA UDI

Category: Dental cement trial

Variolink Esthetic Try In by Ivoclar Vivadent Aktiengesellschaft — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental cement trial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Ivoclar Vivadent Aktiengesellschaft

Sources (1)

  • FDA UDI b88c8681-acb9-4fdb-b1b9-5f4be750e7b9 34 fields · synced May 30, 2026