Primary Device ID | E22114031 |
NIH Device Record Key | 91841a34-147c-442f-b7d2-5167e7af098e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Rebilda DC |
Version Model Number | 1403 |
Catalog Number | 1403 |
Company DUNS | 316699578 |
Company Name | VOCO GmbH |
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 |
Phone | 999-999-9999 |
xxx@xx.xx |
Storage Environment Temperature | Between 4 Degrees Celsius and 23 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
HIBCC | E22114031 [Primary] |
EBF | Material, Tooth Shade, Resin |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-08-31 |
E22114051 | Dual-curing flowable core build-up and post luting system |
E22114041 | Dual-curing flowable core build-up and post luting system |
E22114031 | Dual-curing flowable core build-up and post luting system |
E22114021 | Rebilda DC is a dual-curing, radiopaque, flowable composite indicated for core build-ups |
E22113981 | Dual-curing flowable core build-up and post luting system |
E22113971 | Dual-curing flowable core build-up and post luting system |
E22113961 | Dual-curing flowable core build-up and post luting system |
E22113951 | Rebilda DC is a dual-curing, radiopaque, flowable composite indicated for core build-ups |
E22114061 | Dual-curing flowable core build-up and post luting system |
E22113991 | Dual-curing flowable core build-up and post luting system |