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Cervitec Plus

FDA UDI

Class II (US FDA UDI)

by Ivoclar Vivadent Aktiengesellschaft

Identity

Trade Name
CERVITEC PLUS FDA UDI
Generic Name
Dental coating, tooth-desensitizing, professional FDA UDI
Device Name
Cervitec Plus Test Pack 3x0.25g FDA UDI
Model / Reference
701184AL FDA UDI
Description
Cervitec Plus Test Pack 3x0.25g FDA UDI

Identifiers

Catalog Number
701184 FDA UDI
Primary DI / UDI-DI
DVIV701184AL1 FDA UDI
FDA Product Code
LBH FDA UDI
GMDN Term
Dental coating, tooth-desensitizing, professional FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3260 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

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 coating, tooth-desensitizing, professional

Cervitec Plus by Ivoclar Vivadent Aktiengesellschaft — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental coating, tooth-desensitizing, professional.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b40219e2-928b-4c12-98e8-8463134fac53 34 fields · synced May 30, 2026