Duns Number:533108028
Catalog Number
17000-033-0001
Brand Name
SapphirePlus Infusion Kit - US
Version/Model Number
17000-033-0001
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Unsafe
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
K141389,K141389,K141389,K141389
Product Code
FRN
Product Code Name
Pump, Infusion
Public Device Record Key
51c959d8-46b7-4db8-889f-a199e6fea371
Public Version Date
July 04, 2022
Public Version Number
5
DI Record Publish Date
February 22, 2018
Package DI Number
27290109150226
Quantity per Package
8
Contains DI Package
17290109150229
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
cardboard box
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 65 |