← Back to catalogue

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
Special Fibered #52 Self Curing FDA UDI
Model / Reference
05045-001P FDA UDI
Description
Special Fibered #52 Self Curing FDA UDI

Identifiers

Catalog Number
05045-001P FDA UDI
Primary DI / UDI-DI
B71505045001P0 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
Weight — 1 Pound 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

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

Manufacturer

Sources (1)

  • FDA UDI 41c9971c-283b-4821-99ef-b7339802a4a5 36 fields · synced May 30, 2026