Primary Device ID | 50085412150579 |
NIH Device Record Key | c0123a64-67a9-408e-91d7-ffac5769fd92 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ACID CONCENTRATE |
Version Model Number | 5M8002A |
Catalog Number | 5M8002A |
Company DUNS | 005146311 |
Company Name | BAXTER INTERNATIONAL 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 | true |
OTC Over-The-Counter | false |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com |
Total Volume | 4.5 Liter |
Storage Environment Temperature | Between 25 Degrees Celsius and 0 Degrees Celsius |
Storage Environment Temperature | Between 25 Degrees Celsius and 0 Degrees Celsius |
Storage Environment Temperature | Between 25 Degrees Celsius and 0 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00085412150574 [Primary] |
GS1 | 50085412150579 [Package] Contains: 00085412150574 Package: CASE [4 Units] In Commercial Distribution |
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 | 2015-10-24 |
50085412150623 | Concentrated Hemodialysis Solution |
50085412150616 | Concentrated Hemodialysis Solution |
50085412150593 | Concentrated Hemodialysis Solution |
50085412150586 | Concentrated Hemodialysis Solution |
50085412150579 | Concentrated Hemodialysis Solution |
50085412150562 | Concentrated Hemodialysis Solution |