Duns Number:001307735
Device Description: Corning CellSTACK, 1-layer Polystyrene vessel Closed System for Merck, with Left Port Fill Corning CellSTACK, 1-layer Polystyrene vessel Closed System for Merck, with Left Port Fill Wye, Right Port Vent, with Sartorius Filters, TC treated Growth Surface, Sterile, 1 per bag, 8 per case
Catalog Number
7212
Brand Name
Corning
Version/Model Number
7212
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
KJA
Product Code Name
Flask, tissue culture
Public Device Record Key
c46bc21f-0b74-4054-8a7a-d8ef015c9950
Public Version Date
June 17, 2022
Public Version Number
3
DI Record Publish Date
December 02, 2020
Package DI Number
H10872123
Quantity per Package
8
Contains DI Package
H10872121
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 387 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 2 |