Catalog Number

D1A2

Brand Name

n/a

Version/Model Number

D1A2

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

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K132315

Product Code

EIA

Product Code Name

Unit, Operative Dental

Public Device Record Key

d73aae4f-8e3c-4964-8f3a-2d6c3b3aff3a

Public Version Date

October 24, 2022

Public Version Number

2

DI Record Publish Date

August 19, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-