Primary Device ID | J014660021860 |
NIH Device Record Key | 2d308fcf-716b-4334-acf8-c4be0834e535 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FLEXITIME CORRECT FLOW 1 X (2 X 50 ML) |
Version Model Number | 66002186 |
Catalog Number | 66002186 |
Company DUNS | 315666321 |
Company Name | Heraeus Kulzer GmbH |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
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 | 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 |
Phone | +1(800)431-1785 |
xxx@xxx.xxx | |
Phone | +1(800)431-1785 |
xxx@xxx.xxx | |
Phone | +1(800)431-1785 |
xxx@xxx.xxx | |
Phone | +1(800)431-1785 |
xxx@xxx.xxx | |
Phone | +1(800)431-1785 |
xxx@xxx.xxx | |
Phone | +1(800)431-1785 |
xxx@xxx.xxx | |
Phone | +1(800)431-1785 |
xxx@xxx.xxx | |
Phone | +1(800)431-1785 |
xxx@xxx.xxx | |
Phone | +1(800)431-1785 |
xxx@xxx.xxx | |
Phone | +1(800)431-1785 |
xxx@xxx.xxx | |
Phone | +1(800)431-1785 |
xxx@xxx.xxx | |
Phone | +1(800)431-1785 |
xxx@xxx.xxx | |
Phone | +1(800)431-1785 |
xxx@xxx.xxx | |
Phone | +1(800)431-1785 |
xxx@xxx.xxx | |
Phone | +1(800)431-1785 |
xxx@xxx.xxx | |
Phone | +1(800)431-1785 |
xxx@xxx.xxx | |
Phone | +1(800)431-1785 |
xxx@xxx.xxx |
Device Issuing Agency | Device ID |
---|---|
HIBCC | J014660021860 [Primary] |
ELW | MATERIAL, IMPRESSION |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2023-10-30 |
Device Publish Date | 2016-09-15 |
J014660021861 | Dental Composite resin |
J014660021860 | Material Impression |
J014500348060 | Material, Impression |