MICROARCH®+ - MICROARCH®+ Base Rx 018 UL/5-5 CS HK - DENTSPLY SIRONA ORTHODONTICS INC.

Duns Number:116903307

Device Description: MICROARCH®+ Base Rx 018 UL/5-5 CS HK

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More Product Details

Catalog Number

KJ72-055-13

Brand Name

MICROARCH®+

Version/Model Number

KJ72-055-13

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

February 19, 2021

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)

Yes

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

EJF

Product Code Name

BRACKET, METAL, ORTHODONTIC

Device Record Status

Public Device Record Key

b54ca5fc-94b3-4c0b-851e-fd3fda470037

Public Version Date

February 22, 2021

Public Version Number

3

DI Record Publish Date

September 30, 2019

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"DENTSPLY SIRONA ORTHODONTICS INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 467
2 A medical device with a moderate to high risk that requires special controls. 18