Primary Device ID | J014660398620 |
NIH Device Record Key | 7e4dc445-f221-4fb0-9cf5-541276843398 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | iBOND ETCH 35 GEL 2 x 2,5 ML |
Version Model Number | 66039862 |
Catalog Number | 66039862 |
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 | |
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 | J014660398620 [Primary] |
KLE | AGENT, TOOTH BONDING, RESIN |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2024-02-16 |
Device Publish Date | 2016-09-15 |
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