Duns Number:796452311
Device Description: LW MULTI-LINK,5LEAD,Slw,PINCH,29",BL
Catalog Number
8998
Brand Name
LW MULTI-LINK,5LEAD,Slw,PINCH,29",BL
Version/Model Number
LDW-05BD-29BL-0000
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
October 24, 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
-
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
K081762
Product Code
DSA
Product Code Name
Cable, Transducer And Electrode, Patient, (Including Connector)
Public Device Record Key
39a49ac6-cbee-4db6-a15f-2914d50470f5
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
September 24, 2016
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 478 |
2 | A medical device with a moderate to high risk that requires special controls. | 8062 |