Primary Device ID | EKUR004204KA1 |
NIH Device Record Key | 9f09650b-20e4-4646-adc1-e02c40988af6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PANAVIA SA Cement Universal |
Version Model Number | #4204-KA |
Company DUNS | 697119498 |
Company Name | KURARAY NORITAKE DENTAL INC. |
Device Count | 1 |
DM Exempt | false |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | EKUR004204KA1 [Primary] |
KLE | Agent, Tooth Bonding, Resin |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-07-01 |
Device Publish Date | 2019-06-21 |
EKUR004221KA1 | Automix Endo tip (SS) |
EKUR004218KA1 | Automix Mixing tip |
EKUR004217KA1 | Automix Trial (Translucent) |
EKUR004216KA1 | Automix Trial (Universal (A2)) |
EKUR004214KA1 | Automix (Translucent) |
EKUR004213KA1 | Automix (White) |
EKUR004212KA1 | Automix (Universal (A2)) |
EKUR004211KA1 | Automix Value Pack (Translucent) |
EKUR004210KA1 | Automix Value Pack (Universal (A2)) |
EKUR004204KA1 | Handmix (Translucent) |
EKUR004203KA1 | Handmix (White) |
EKUR004202KA1 | Handmix (Universal (A2)) |