Primary Device ID | E22110601 |
NIH Device Record Key | e6b24c94-586b-4031-9946-91a5fade0478 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Grandio Seal |
Version Model Number | 1060 |
Catalog Number | 1060 |
Company DUNS | 316699578 |
Company Name | VOCO GmbH |
Device Count | 5 |
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 | E2211060 [Unit of Use] |
HIBCC | E22110601 [Primary] |
EBC | Sealant, Pit And Fissure, And Conditioner |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-06-13 |
Device Publish Date | 2019-06-05 |
E22110611 | Grandio® Seal is a light-curing, highly filled, fluoride-containing nanohybrid fissure sealant |
E22110601 | Grandio® Seal is a light-curing, highly filled, fluoride-containing nanohybrid fissure sealant |