Power Dental U.S.A., Inc. - EXP 23 S/E, 1EZ, ENGRAVE 20-EXP 23 - Power Dental U.S.A. Inc.

Duns Number:081305064

Device Description: EXP 23 S/E, 1EZ, ENGRAVE 20-EXP 23

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More Product Details

Catalog Number

NMM1005

Brand Name

Power Dental U.S.A., Inc.

Version/Model Number

NMM1005

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

June 17, 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

EKB

Product Code Name

EXPLORER, OPERATIVE

Device Record Status

Public Device Record Key

879d187d-f3c8-41b3-b81b-a3beb3977c6d

Public Version Date

June 21, 2022

Public Version Number

2

DI Record Publish Date

June 20, 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