Primary Device ID | D003CD20120 |
NIH Device Record Key | e847f21e-2c91-48d9-b78a-61042616d4eb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Purevac® HVE |
Version Model Number | CD20012 |
Catalog Number | CD2012 |
Company DUNS | 144140845 |
Company Name | Dentsply Professional |
Device Count | 12 |
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 | true |
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 |
Device Issuing Agency | Device ID |
---|---|
HIBCC | D003CD20120 [Unit of Use] |
HIBCC | D003CD20121 [Primary] |
EHZ | Evacuator, oral cavity |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-12-12 |
Device Publish Date | 2022-12-03 |
D003CD20120 | Purevac® HVE Mirror Tips 12 FS Rhodium |
D003CD20060 | Purevac® HVE Mirror Tips 6 FS Rhodium |
D003110200 | Purevac® HVE Mirror Tips – 12 pack |
D003110100 | Purevac® HVE Mirror Tips – 3 pack |
D003110001 | Purevac® HVE System Kit |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PUREVAC 74292772 1776176 Live/Registered |
DENTSPLY SIRONA INC. 1992-07-10 |
PUREVAC 74033556 not registered Dead/Abandoned |
Parker Netsushori Kogyo K. K. 1990-03-01 |