Catalog Number

26059

Brand Name

DLA,6 LEAD,SNAP,MULTILINK,MOLDED,40",AHA

Version/Model Number

DLA-06AD-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

40425cb2-425d-4964-ba00-58f39885657f

Public Version Date

April 30, 2020

Public Version Number

1

DI Record Publish Date

April 22, 2020

Package DI Number

90840828180088

Quantity per Package

2

Contains DI Package

90840828180071

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-