Duns Number:797372554
Device Description: Surface area 1.9m² Max.TMP:66kPa(500mmHg)
Catalog Number
DD+ELISIO-19H
Brand Name
NIPRO ELISIO™ -H HEMODIALYZER
Version/Model Number
ELISIO™-19H
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
KDI
Product Code Name
Dialyzer, high permeability with or without sealed dialysate system
Public Device Record Key
309f79a4-ae47-40c8-be3f-94f1295ae85d
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
September 16, 2015
Package DI Number
40383790007113
Quantity per Package
24
Contains DI Package
00383790007115
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Case
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 230 |