Catalog Number

620-030-301

Brand Name

NA

Version/Model Number

0620030301

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

NKC

Product Code Name

Tubing/tubing with filter, insufflation, laparoscopic

Public Device Record Key

7a69d267-8e1d-423a-83a7-4dc767bd05f1

Public Version Date

December 24, 2019

Public Version Number

1

DI Record Publish Date

December 16, 2019

Package DI Number

37613327055604

Quantity per Package

10

Contains DI Package

07613327055603

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

pack