Duns Number:008254708
Device Description: LabPro Data Management System
Catalog Number
-
Brand Name
MicroScan
Version/Model Number
V4.42MUA
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
-
Product Code
OUG
Product Code Name
Medical Device Data System
Public Device Record Key
7bc84f72-4803-425c-9000-1669915124cf
Public Version Date
September 16, 2022
Public Version Number
4
DI Record Publish Date
November 07, 2016
Package DI Number
15099590684105
Quantity per Package
1
Contains DI Package
15099590684068
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
6000-0072
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 319 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 503 |
| 3 | A medical device with high risk that requires premarket approval | 9 |
| U | Unclassified | 1 |