Primary Device ID | 14573316385558 |
NIH Device Record Key | 18d4d736-cc95-43a0-a1fc-0dd9d370f6ca |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DS(Diluent Solution) Pack 4 vials |
Version Model Number | VT602US-DSx4 |
Catalog Number | 91245 |
Company DUNS | 711091157 |
Company Name | KITAZATO 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 | true |
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 |