Duns Number:187129135
Device Description: Kit includes:CTR22, 5x100 Kii LP OPT ZTHR 6/BXCTF73, Kii 12x100 Fios Z-THR 6/BXC0R47, 12x1 Kit includes:CTR22, 5x100 Kii LP OPT ZTHR 6/BXCTF73, Kii 12x100 Fios Z-THR 6/BXC0R47, 12x100 Kii BALLOON BLUNT TIP 6/BXC6003, VALVE WITH DUAL BAG TUBING, 12/BX
Catalog Number
-
Brand Name
Standard Set 400 Z
Version/Model Number
CK101
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
Yes
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
FHF
Product Code Name
System, Evacuator, Fluid
Public Device Record Key
913225f0-b276-4e83-98d9-c223208d1740
Public Version Date
January 09, 2020
Public Version Number
5
DI Record Publish Date
September 24, 2016
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 | 499 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 698 |
| 3 | A medical device with high risk that requires premarket approval | 1 |