Duns Number:421355284
Catalog Number
-
Brand Name
Medicpad
Version/Model Number
AS1080
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
October 05, 2022
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)
-
Over the Counter (OTC)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K143268,K143268
Product Code
NGX
Product Code Name
Stimulator, Muscle, Powered, For Muscle Conditioning
Public Device Record Key
6bee6118-2e05-4407-ad90-a849c2fffb5a
Public Version Date
October 05, 2022
Public Version Number
11
DI Record Publish Date
March 07, 2017
Package DI Number
06970890321704
Quantity per Package
36
Contains DI Package
06970890320110
Package Discontinue Date
May 18, 2021
Package Status
Not in Commercial Distribution
Package Type
Carton
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 13 |