Primary Device ID | D949301021101 |
NIH Device Record Key | f76d18c8-e3a3-4ed5-9e60-5ad8bab88248 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Original Anterior Matrix A Series |
Version Model Number | A102 |
Company DUNS | 059020838 |
Company Name | Bioclear Matrix Systems |
Device Count | 25 |
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 | D949301021101 [Unit of Use] |
HIBCC | D949301021251 [Primary] |
HIBCC | D949301021501 [Primary] |
JEP | Retainer, Matrix |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-08-22 |
Device Publish Date | 2023-08-14 |
D9493010110 | Clear matrix used in dental restorations. |
D949301021101 | Clear matrix used in dental restorations. |
D9493010510 | Clear matrix used in dental restorations. |
D9493010410 | Clear matrix used in dental restorations. |
D9493010310 | Clear matrix used in dental restorations. |
D9493010210 | Clear matrix used in dental restorations. |