Dual-Force™ Sectional Matrix System Starter Kit w/ Ultra-Wrap - Collection of devices for direct restoration - CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.

Duns Number:626406016

Device Description: Collection of devices for direct restoration procedures

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More Product Details

Catalog Number

209021

Brand Name

Dual-Force™ Sectional Matrix System Starter Kit w/ Ultra-Wrap

Version/Model Number

209021

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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)

-

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

DZN

Product Code Name

INSTRUMENTS, DENTAL HAND

Device Record Status

Public Device Record Key

1db60d14-2231-4ad3-9d01-e69087968a52

Public Version Date

August 20, 2021

Public Version Number

1

DI Record Publish Date

August 12, 2021

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"CLINICIAN'S CHOICE DENTAL PRODUCTS, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 1461
2 A medical device with a moderate to high risk that requires special controls. 234
U Unclassified 6