Primary Device ID | 10817411022418 |
NIH Device Record Key | 2a48c8e6-10e0-497f-9c6c-e7c5705ff69d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MedicaLyte |
Version Model Number | DB+201-15 |
Company DUNS | 117439434 |
Company Name | NIPRO RENAL SOLUTIONS USA CORPORATION |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817411022411 [Primary] |
GS1 | 10817411022418 [Package] Contains: 00817411022411 Package: Case [3 Units] In Commercial Distribution |
KPO | Dialysate Concentrate For Hemodialysis (Liquid Or Powder) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-10-07 |
Device Publish Date | 2020-09-29 |
10817411022821 | Liquid Bicarbonate Concentrate for Hemodialysis |
10817411022418 | Dry Bicarbonate Powder Concentrate for Hemodialysis |
10817411022401 | Dry Bicarbonate Powder Concentrate for Hemodialysis |
10817411022395 | Dry Bicarbonate Powder Concentrate for Hemodialysis |
10817411022814 | Liquid Bicarbonate Concentrate |
10817411022807 | Dry Bicarbonate Powder Concentrate |
10817411022791 | Dry Bicarbonate Powder Concentrate |
10817411022784 | Dry Bicarbonate Powder Concentrate |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MEDICALYTE 97440242 not registered Live/Pending |
NIPRO CORPORATION 2022-06-02 |