Primary Device ID | 00841543143799 |
NIH Device Record Key | 7f791236-b60a-4f18-b00b-edfef16ca4c0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | O'NEILL |
Version Model Number | ONS-ENSENADA2.0-106P |
Company DUNS | 845937478 |
Company Name | Inspecs U.S.A., L.C. |
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 | false |
Lot Batch | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |