Primary Device ID | 08800099966131 |
NIH Device Record Key | 55c0295e-4ae6-49b9-8fdd-12e9acc8c61e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Perfit FS |
Version Model Number | FH I12 A3 |
Company DUNS | 688284886 |
Company Name | Vatech mcis Co., Ltd |
Device Count | 5 |
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 |