Power Dental USA - ASDF - Power Dental U.S.A. Inc.

Duns Number:081305064

Device Description: ASDF

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More Product Details

Catalog Number

1313

Brand Name

Power Dental USA

Version/Model Number

1313

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

June 16, 2022

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"

Yes

For Single-Use

-

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

EID

Product Code Name

SYRINGE, RESTORATIVE AND IMPRESSION MATERIAL

Device Record Status

Public Device Record Key

02820b21-f3d3-46e1-a5f2-645c082a1d39

Public Version Date

June 17, 2022

Public Version Number

3

DI Record Publish Date

July 13, 2021

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"POWER DENTAL U.S.A. INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 2768
2 A medical device with a moderate to high risk that requires special controls. 18