Primary Device ID | 10810138823092 |
NIH Device Record Key | 2e4c3ab0-fc12-40f5-b822-5b1fd3859fba |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ProShape Paper Points ISO 30.04 |
Version Model Number | PSPP3004 |
Company DUNS | 125216703 |
Company Name | Endo Direct LLC |
Device Count | 1 |
DM Exempt | true |
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 | 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 | true |
OTC Over-The-Counter | false |