Primary Device ID | 00814963020063 |
NIH Device Record Key | d3c06147-5cc9-4174-9912-1d62c066f18d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RenalPure |
Version Model Number | FB-25-2 |
Catalog Number | FB-25 |
Company DUNS | 933721433 |
Company Name | ROCKWELL MEDICAL, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00814963020063 [Primary] |
KPO | Dialysate Concentrate For Hemodialysis (Liquid Or Powder) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-09-22 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
RENALPURE 76539654 3029776 Live/Registered |
ROCKWELL MEDICAL, INC. 2003-08-25 |