Catalog Number

-

Brand Name

Irrigation line, W&H

Version/Model Number

32.F0084.00

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

EFS

Product Code Name

Unit, Oral Irrigation

Public Device Record Key

cfcc6105-c210-4b2d-9ae5-ad88ae1d4ca2

Public Version Date

February 28, 2022

Public Version Number

1

DI Record Publish Date

February 18, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-