Primary Device ID | 00348783004564 |
NIH Device Record Key | 4f0d16fa-6180-4ec5-befe-cfb6d69cb9a2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ProFlare |
Version Model Number | 5500193 |
Company DUNS | 014789663 |
Company Name | PREMIER DENTAL PRODUCTS COMPANY |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 |
---|---|
GS1 | 00348783004564 [Primary] |
EHK | Cup, Prophylaxis |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-11-03 |
Device Publish Date | 2023-10-26 |
00348783004564 | ProFlare Articulating Disposable Prophy Angle Sample |
00348783001181 | ProFlare Articulating DPA (Bag of 125) |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PROFLARE 97771096 not registered Live/Pending |
Premier Dental Products Company 2023-01-27 |
PROFLARE 78847147 3343969 Dead/Cancelled |
Proflare, Inc. 2006-03-27 |
PROFLARE 78523751 not registered Dead/Abandoned |
Proflare, Inc 2004-11-29 |