Primary Device ID | 08800118609902 |
NIH Device Record Key | 9c909016-a27c-4d68-9a6f-41d3042d112f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Razor / MegaPlus |
Version Model Number | W 1100 C2 22 |
Company DUNS | 694821663 |
Company Name | U&C International Co.,Ltd |
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 | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |