Duns Number:079226220
Device Description: ARCHITECT Transplant Pretreatment Tubes
Catalog Number
01P0602
Brand Name
ARCHITECT
Version/Model Number
1P06-02
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
K070820,K070822,K080751,K070820,K070822,K080751
Product Code
MKW
Product Code Name
CYCLOSPORINE
Public Device Record Key
336785b3-3eec-4964-b710-ecf598f613f2
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
September 09, 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 | 259 |
2 | A medical device with a moderate to high risk that requires special controls. | 245 |
U | Unclassified | 5 |