Primary Device ID | 80028373149986 |
NIH Device Record Key | e7cf04dc-3195-4223-a505-38cdc641dc7f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | WINK CLOSER |
Version Model Number | 14998 |
Company DUNS | 175752724 |
Company Name | OKAMOTO USA, INC. |
Device Count | 1008 |
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 | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |