Catalog Number

LS7012

Brand Name

MD Resource

Version/Model Number

LS7012

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

248f4be1-7be2-4ad5-a1be-8ccda0c891c6

Public Version Date

June 08, 2021

Public Version Number

5

DI Record Publish Date

August 30, 2016

Package DI Number

00859898006133

Quantity per Package

4

Contains DI Package

00859898006126

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-