Duns Number:448015938
Device Description: Astropol P Refill 6
Catalog Number
557620
Brand Name
Astropol
Version/Model Number
557620
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
November 05, 2021
Issuing Agency
In HIBCC
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
EHJ
Product Code Name
DISK, ABRASIVE
Public Device Record Key
ac44208e-0a5d-4704-b026-293e0d485bdd
Public Version Date
November 08, 2021
Public Version Number
2
DI Record Publish Date
August 26, 2020
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 | 131 |
2 | A medical device with a moderate to high risk that requires special controls. | 12768 |