Duns Number:377142935
Device Description: Laboratory freezer
Catalog Number
991.8836.01
Brand Name
B Medical Systems
Version/Model Number
F900
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
February 10, 2020
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)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
JRM
Product Code Name
Freezer
Public Device Record Key
08e4667e-2aff-4ac1-b019-34fd7eaaea3f
Public Version Date
February 11, 2020
Public Version Number
2
DI Record Publish Date
February 08, 2019
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 | 104 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 104 |