Catalog Number

18590

Brand Name

DISP ECG LW,5LD,SNAP,TW PIN,AHA,INTERMED

Version/Model Number

DLW-05AB-40AS-3000

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

December 28, 2017

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

36ea52da-fa4d-483a-8cab-00af29841a3a

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 24, 2016

Package DI Number

90840828101076

Quantity per Package

10

Contains DI Package

90840828100925

Package Discontinue Date

December 28, 2017

Package Status

Not in Commercial Distribution

Package Type

-