Primary Device ID | 20749915001668 |
NIH Device Record Key | 26f57779-e390-478f-9bae-a4b1dad163e8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cylindrical Sponge |
Version Model Number | 70-02 |
Company DUNS | 151054954 |
Company Name | AMERICAN SURGICAL COMPANY, LLC |
Device Count | 50 |
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 | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |