Primary Device ID | 07615208469929 |
NIH Device Record Key | 0f9e6ca2-d0fc-4c93-8560-8cc0a0524c6c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tetric PowerFlow |
Version Model Number | 692414WW |
Catalog Number | 692414WW |
Company DUNS | 448015938 |
Company Name | IVOCLAR VIVADENT AKTIENGESELLSCHAFT |
Device Count | 20 |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07615208293524 [Primary] |
GS1 | 07615208469929 [Unit of Use] |
HIBCC | DVIV692414WW1 [Previous] |
EBF | Material, tooth shade, 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 | 2023-03-31 |
Device Publish Date | 2023-03-23 |
DVIV692417WW1 | Tetric PowerFlow Test Pack 1x1.3g IVA |
DVIV692411WW1 | Tetric PowerFlow Refill 1 x 2g IVW |
DVIV692410WW1 | Tetric PowerFlow Refill 1 x 2g IVB |
DVIV692409WW1 | Tetric PowerFlow Refill 1 x 2g IVA |
DVIV692414WW1 | Tetric PowerFlow Refill 20 x 0.2g IVB |
DVIV692413WW1 | Tetric PowerFlow Refill 20 x 0.2g IVA |
07615208458190 | Tetric PowerFlow Test Pack 1x1.3g IVA |
07615208293555 | Tetric PowerFlow Refill 1 x 2g IVB |
07615208293548 | Tetric PowerFlow Refill 1 x 2g IVW |
07615208469912 | Tetric PowerFlow Refill 20 x 0.2g IVA |
07615208469929 | Tetric PowerFlow Refill 20 x 0.2g IVB |
07615208469936 | Tetric PowerFlow Refill 20 x 0.2g IVW |
07615208464276 | Tetric PowerFlow/Cannula Refill |