Primary Device ID | 08800118601753 |
NIH Device Record Key | 50c215b2-50e6-40f0-b84f-f52f7a89a453 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Everest / MegaPlus |
Version Model Number | 5188 LT WH 98-25 |
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 |