Catalog Number

DIL-501-19

Brand Name

Dilator

Version/Model Number

DIL-501-19

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"

Yes

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

DYB

Product Code Name

Introducer, Catheter

Public Device Record Key

be9e4eb9-4002-405e-8ed5-d7f1467e2da0

Public Version Date

June 14, 2021

Public Version Number

1

DI Record Publish Date

June 04, 2021

Package DI Number

10841268109459

Quantity per Package

5

Contains DI Package

00841268109452

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Shelf Box