Primary Device ID | D00116936LT11D0 |
NIH Device Record Key | 55841f03-5421-4f6f-b635-ec899d24d856 |
Commercial Distribution Discontinuation | 2022-05-05 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Trublend® SLM® Anteriors |
Version Model Number | T11 L D |
Catalog Number | 16936 |
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 | true |
Lot Batch | true |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | D00116936LT11D0 [Primary] |
ELM | Denture, plastic, teeth |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2023-12-13 |
Device Publish Date | 2016-10-10 |