Duns Number:006261481
Device Description: CUSTOM PACK SSBB10N21R 10PK SUPPLEMENT P
Catalog Number
-
Brand Name
NA
Version/Model Number
SSBB10N21R
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
October 21, 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
DWF
Product Code Name
Catheter, cannula and tubing, vascular, cardiopulmonary bypass
Public Device Record Key
57c23c5c-8b2f-43a6-8048-129aa1928b6a
Public Version Date
March 01, 2022
Public Version Number
3
DI Record Publish Date
May 24, 2018
Package DI Number
20763000146775
Quantity per Package
10
Contains DI Package
00763000146764
Package Discontinue Date
October 21, 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 |