Duns Number:123738960
Device Description: 10.8V 800MAH NICD W/LEADS
Catalog Number
-
Brand Name
Interstate All Battery
Version/Model Number
MED0014
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
August 09, 2019
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
Yes
Prescription Use (Rx)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
MOQ
Product Code Name
Battery, Replacement, Rechargeable
Public Device Record Key
78b3d0ad-8354-4fdc-806b-5ec98c1a9b59
Public Version Date
August 12, 2019
Public Version Number
3
DI Record Publish Date
March 19, 2018
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 | 154 |