Primary Device ID | D0019062200 |
NIH Device Record Key | 2c4211f8-bc44-4f64-839c-54670c9c67d0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Lucitone Digital Try-In™ |
Version Model Number | 3D Trial Placement Resin - A1 |
Catalog Number | 906220 |
Company DUNS | 606173334 |
Company Name | Dentsply International 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 | true |
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 |
Weight | 1 Kilogram |
Weight | 1 Kilogram |
Weight | 1 Kilogram |
Weight | 1 Kilogram |
Weight | 1 Kilogram |
Weight | 1 Kilogram |
Weight | 1 Kilogram |
Weight | 1 Kilogram |
Weight | 1 Kilogram |
Weight | 1 Kilogram |
Weight | 1 Kilogram |
Weight | 1 Kilogram |
Weight | 1 Kilogram |
Weight | 1 Kilogram |
Weight | 1 Kilogram |
Weight | 1 Kilogram |
Device Issuing Agency | Device ID |
---|---|
HIBCC | D0019062200 [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 | 2019-09-17 |
Device Publish Date | 2019-09-09 |
D0019062250 | 3D Trial Placement Resin - BL3 |
D0019062240 | 3D Trial Placement Resin - B2 |
D0019062230 | 3D Trial Placement Resin - B1 |
D0019062220 | 3D Trial Placement Resin - A3 |
D0019062210 | 3D Trial Placement Resin - A2 |
D0019062200 | 3D Trial Placement Resin - A1 |