PROPHY PASTE - MAXILL, INC.

Duns Number:079343581

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More Product Details

Catalog Number

-

Brand Name

PROPHY PASTE

Version/Model Number

6070540562

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

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code Details

Product Code

EJR

Product Code Name

Agent, Polishing, Abrasive, Oral Cavity

Device Record Status

Public Device Record Key

ef35a996-9267-468c-8e84-436c5b873b71

Public Version Date

October 28, 2022

Public Version Number

1

DI Record Publish Date

October 20, 2022

Additional Identifiers

Package DI Number

D89260705405622

Quantity per Package

4000

Contains DI Package

D89260705405621

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case

"MAXILL, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 208
2 A medical device with a moderate to high risk that requires special controls. 61