Catalog Number

24570

Brand Name

DLA,5 LEAD,SNAP,MULTILINK,MOLDED,40",AHA

Version/Model Number

DLA-05AD-40AM-0000

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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

DSA

Product Code Name

Cable, Transducer And Electrode, Patient, (Including Connector)

Public Device Record Key

ee7511d3-120f-46fd-afc8-1509f83b61d4

Public Version Date

April 30, 2020

Public Version Number

1

DI Record Publish Date

April 22, 2020

Package DI Number

90840828179983

Quantity per Package

2

Contains DI Package

90840828174797

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-