Duns Number:080242300
Device Description: REUSABLE ULTRALAST CUP ELECTRODES: 9 MM MOLDED SILVER DISC, 6 FT. (1.8 M), SINGLE, KEVLAR REUSABLE ULTRALAST CUP ELECTRODES: 9 MM MOLDED SILVER DISC, 6 FT. (1.8 M), SINGLE, KEVLAR WIRE
Catalog Number
-
Brand Name
UltraLast
Version/Model Number
DE-BMS042T15-6
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"
-
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
K142159
Product Code
GXY
Product Code Name
Electrode, Cutaneous
Public Device Record Key
b46270e3-e0e3-4edf-9296-b217c2515d9e
Public Version Date
April 18, 2019
Public Version Number
1
DI Record Publish Date
April 10, 2019
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 |
|---|---|---|
| 2 | A medical device with a moderate to high risk that requires special controls. | 1261 |