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Vitacrilic®

FDA UDI

Class II (US FDA UDI)

by Fricke International, Inc.

Identity

Trade Name
Vitacrilic® FDA UDI
Generic Name
Dental appliance fabrication material, resin FDA UDI
Device Name
Clear Pour Monomer FDA UDI
Model / Reference
9090-00 FDA UDI
Description
Clear Pour Monomer FDA UDI

Identifiers

Catalog Number
9090-00 FDA UDI
Primary DI / UDI-DI
B7159090000 FDA UDI
FDA Product Code
EBI FDA UDI
GMDN Term
Dental appliance fabrication material, resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3760 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Total Volume — 940 Milliliter FDA UDI

Category: Dental appliance fabrication material, resin

Vitacrilic® by Fricke International, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, resin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1d2aef2e-4033-42a5-8fa8-e9366fad7058 36 fields · synced May 30, 2026