Catalog Number

DYNDA2151

Brand Name

MEDLINE

Version/Model Number

DYNDA2151

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

BYY

Product Code Name

TUBE, ASPIRATING, FLEXIBLE, CONNECTING

Public Device Record Key

6c930a47-44cf-4bc6-8da9-81672f153370

Public Version Date

June 08, 2021

Public Version Number

2

DI Record Publish Date

April 03, 2020

Package DI Number

40889942776789

Quantity per Package

30

Contains DI Package

10889942776788

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE