Primary Device ID | D832600BSF4000 |
NIH Device Record Key | a0c923a4-5f71-419f-aa4c-d0264d0ecbeb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MAXAPPLICATOR II |
Version Model Number | 600B-SF-400 |
Catalog Number | 600B-SF-400 |
Company DUNS | 190377184 |
Company Name | PLASDENT CORPORATION |
Device Count | 400 |
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 | 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 | false |