Primary Device ID | D9491120510 |
NIH Device Record Key | 4d79589a-d2fe-45c8-b025-3bbd3fa57e78 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bioclear Diamond Wedge |
Version Model Number | Deep Caries |
Company DUNS | 059020838 |
Company Name | Bioclear Matrix Systems |
Device Count | 50 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 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 | D9491120510 [Unit of Use] |
HIBCC | D949112051021 [Primary] |
HIBCC | D949112051041 [Primary] |
HIBCC | D949112051081 [Primary] |
HIBCC | D949112051101 [Primary] |
HIBCC | D949112051161 [Primary] |
HIBCC | D94911205116KC1 [Primary] |
HIBCC | D949112051500BG1 [Primary] |
HIBCC | D949112051501 [Primary] |
HIBCC | D949112051503 [Primary] |
HIBCC | D94911205150BG1 [Primary] |
EJB | Handle, Instrument, Dental |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-08-15 |
Device Publish Date | 2023-08-07 |
D9491120510 | Plastic wedge used in dental restorations. |
D9491120410 | Plastic wedge used in dental restorations. |
D9491120310 | Plastic wedge used in dental restorations. |
D9491120210 | Plastic wedge used in dental restorations. |
D949112011501 | Plastic wedge used in dental restorations. |
D9491120110 | Plastic wedge used in dental restorations. |