Primary Device ID | 00814963020605 |
NIH Device Record Key | 55ecaea8-7694-48a5-aa8a-45d1ecf4b193 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DriSate |
Version Model Number | DF-140 |
Catalog Number | DF-140 |
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 | 00814963020605 [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 | 2015-09-18 |
00814963021404 | DF-113 |
00814963021398 | DF-112 |
00814963021381 | DF-111 |
00814963020698 | DR-250 |
00814963020681 | DR-245 |
00814963020674 | DR-230 |
00814963020667 | DR-210 |
00814963020650 | DR-145 |
00814963020643 | DR-130 |
00814963020636 | DR-120 |
00814963020629 | DF-240 |
00814963020612 | DF-220 |
00814963020605 | DF-140 |
00814963020599 | DF-125 |
00814963020582 | DF-120 |
00814963020575 | DF-115 |
00814963020568 | DC-124 |
00814963020551 | DC-117 |
00814963020544 | DC-116 |
00814963020537 | DC-114 |
00814963020520 | DC-110 |
00814963020513 | DC-108 |
00814963020506 | DC-109 |
00814963020490 | DC-103 |