Primary Device ID | E22116261 |
NIH Device Record Key | dba65d1e-ae39-497f-a885-d52cd2e73e01 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Quick Up |
Version Model Number | 1626 |
Catalog Number | 1626 |
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 | E22116261 [Primary] |
EBI | Resin, Denture, Relining, Repairing, Rebasing |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-08-09 |
Device Publish Date | 2016-08-31 |
E22116281 | 1628 |
E22116261 | Self-curing luting material for attachments and secondary denture parts |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() QUICK UP 98231367 not registered Live/Pending |
Absorbent Specialty Products, LLC 2023-10-19 |
![]() QUICK UP 79101798 4116852 Live/Registered |
VOCO GmbH 2011-06-10 |
![]() QUICK UP 73512073 1344140 Live/Registered |
NATIONAL UNION ELECTRIC CORPORATION 1984-12-05 |