Primary Device ID | D7911900B2500 |
NIH Device Record Key | 08fda07d-38cf-4f6e-8bba-541b95d8219e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Luminesse Low Fusing Porcelain |
Version Model Number | 1900B250 |
Company DUNS | 094430642 |
Company Name | TALLADIUM, 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 | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | D7911900B2500 [Primary] |
EIH | Powder, Porcelain |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-07-24 |
Device Publish Date | 2016-10-24 |
D7911900T1500 | 1900T150 |
D7911900ST4500 | 1900ST450 |
D7911900ST3500 | 1900ST350 |
D7911900ST2500 | 1900ST250 |
D7911900ST1500 | 1900ST150 |
D7911900D4500 | 1900D450 |
D7911900D3500 | 1900D350 |
D7911900C4500 | 1900C450 |
D7911900C3500 | 1900C350 |
D7911900C2500 | 1900C250 |
D7911900C1500 | 1900C150 |
D7911900B4500 | 1900B450 |
D7911900B3500 | 1900B350 |
D7911900B2500 | 1900B250 |
D7911900B1500 | 1900B150 |
D7911900B0500 | 1900B050 |
D7911900B00500 | 1900B0050 |
D7911900A4500 | 1900A450 |
D7911900A35500 | 1900A3550 |
D7911900A3500 | 1900A350 |
D7911900A2500 | 1900A250 |
D7911900A1500 | 1900A150 |
D7911900A0500 | 1900A050 |
D7911900A00500 | 1900A0050 |