Primary Device ID | 08800099966247 |
NIH Device Record Key | 2f40d232-8356-4251-b55e-5d36648bdc9f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Perfit FS |
Version Model Number | FH I12 D2 |
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 |