UNIFAST™ - UNIFAST™ LC Translucent, 50g powder - Gc America Inc.

Duns Number:005473608

Device Description: UNIFAST™ LC Translucent, 50g powder

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More Product Details

Catalog Number

338203

Brand Name

UNIFAST™

Version/Model Number

338203

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K890829,K890829

Product Code Details

Product Code

EBG

Product Code Name

CROWN AND BRIDGE, TEMPORARY, RESIN

Device Record Status

Public Device Record Key

c0e121c9-3f6e-4416-bf9f-bb51a6595fa7

Public Version Date

October 29, 2021

Public Version Number

4

DI Record Publish Date

August 01, 2016

Additional Identifiers

Package DI Number

D6583382032

Quantity per Package

5

Contains DI Package

D6583382031

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton

"GC AMERICA INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 480
2 A medical device with a moderate to high risk that requires special controls. 4772