Primary Device ID | 10878799003611 |
NIH Device Record Key | 86abdf4c-38e3-423d-b997-544c7446c4e7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SURGISTAR |
Version Model Number | 962201 |
Company DUNS | 808865125 |
Company Name | SURGISTAR, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |