Duns Number:276816717
Device Description: Reagents associated to API 20 E™ (20 100/20 160), API® 10 S (10 100), API® 20 NE (20 050), Reagents associated to API 20 E™ (20 100/20 160), API® 10 S (10 100), API® 20 NE (20 050), API® Staph (20 500), API® Coryne (20 900), API® Campy (20 800), ID 32 STAPH (32 500), rapid ID 32 A (32 300)
Catalog Number
-
Brand Name
API® NIT1 NIT2
Version/Model Number
70442
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
JTO
Product Code Name
DISCS, STRIPS AND REAGENTS, MICROORGANISM DIFFERENTIATION
Public Device Record Key
01152db7-1fbe-4b13-badd-d3bf3aca1849
Public Version Date
April 20, 2020
Public Version Number
1
DI Record Publish Date
April 10, 2020
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 | 82 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 156 |
| 3 | A medical device with high risk that requires premarket approval | 3 |