Catalog Number

-

Brand Name

Posterior Band Removing

Version/Model Number

100-171

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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

JEX

Product Code Name

PLIER, ORTHODONTIC

Public Device Record Key

e55df6c3-b008-4ef6-a4fe-6ba84d1218c0

Public Version Date

April 23, 2021

Public Version Number

1

DI Record Publish Date

April 15, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-