| Primary Device ID | 10817411022784 |
| NIH Device Record Key | 3894ffbb-54fa-476a-aeb9-6d3573d275bf |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MedicaLyte |
| Version Model Number | DB+100-2.5 |
| 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 | 00817411022787 [Primary] |
| GS1 | 10817411022784 [Package] Contains: 00817411022787 Package: Case [20 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 | 2022-02-25 |
| Device Publish Date | 2022-02-17 |
| 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 |