Duns Number:884513334
Device Description: U.S. IFU, Manual & CDs, BioPlex 2200 ToRC IgM IFU SW4.3_v1
Catalog Number
12005791
Brand Name
BioPlex 2200
Version/Model Number
4.3_v1
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
LFZ
Product Code Name
ENZYME LINKED IMMUNOABSORBENT ASSAY, CYTOMEGALOVIRUS
Public Device Record Key
308f257b-2730-459a-9ddc-70d14ad85a6a
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
August 05, 2017
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 | 511 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 428 |
| U | Unclassified | 1 |