Duns Number:006261481
Device Description: CUSTOM PACK CB10X91R1 10PK E. SHUNT
Catalog Number
-
Brand Name
NA
Version/Model Number
CB10X91R1
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
June 27, 2019
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
K171308,K171308
Product Code
DTZ
Product Code Name
OXYGENATOR, CARDIOPULMONARY BYPASS
Public Device Record Key
b69b4618-9ec5-4c79-b716-2b651c81e480
Public Version Date
March 01, 2022
Public Version Number
2
DI Record Publish Date
April 14, 2019
Package DI Number
20763000258089
Quantity per Package
10
Contains DI Package
00763000258078
Package Discontinue Date
June 27, 2019
Package Status
Not in Commercial Distribution
Package Type
PK
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 102 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 20495 |
| 3 | A medical device with high risk that requires premarket approval | 3601 |