Primary Device ID | 04540217059478 |
NIH Device Record Key | 8f8d5fa6-421d-445c-a968-fd623924a505 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 0.7/1.3U163C-36 |
Version Model Number | 582-24780-62 |
Company DUNS | 690558747 |
Company Name | SHIMADZU CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |