Primary Device ID | D7915215Z0 |
NIH Device Record Key | f761ff4a-1af6-4671-b4c5-47794477daf0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Luminesse Clear PMMA Discs |
Version Model Number | 5215Z |
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 | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | D7915215Z0 [Primary] |
EBG | Crown And Bridge, Temporary, 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 | 2016-10-24 |
D791CPMMAEX98300 | CPMMAEX9830 |
D791CPMMAEX98250 | CPMMAEX9825 |
D791CPMMAEX98210 | CPMMAEX9821 |
D791CPMMAEX98200 | CPMMAEX9820 |
D791CPMMAEX98100 | CPMMA-EX-98-10 |
D79152290 | 5229 |
D79152250 | 5225 |
D79152240 | 5224 |
D7915223Z0 | 5223Z |
D79152230 | 5223 |
D7915222Z0 | 5222Z |
D79152220 | 5222 |
D79152210 | 5221 |
D79152200 | 5220 |
D79152190 | 5219 |
D79152180 | 5218 |
D79152170 | 5217 |
D7915216Z0 | 5216Z |
D79152160 | 5216 |
D7915215Z0 | 5215Z |
D79152150 | 5215 |
D7915214Z0 | 5214Z |
D79152140 | 5214 |
D7915213Z0 | 5213Z |
D79152130 | 5213 |
D7915212Z0 | 5212Z |
D79152120 | 5212 |