Primary Device ID | D89260705405712 |
NIH Device Record Key | eaa30663-bf6f-47f3-bc70-c9b70f660b9c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PROPHY PASTE |
Version Model Number | 6070540571 |
Company DUNS | 079343581 |
Company Name | MAXILL, INC. |
Device Count | 200 |
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 | D89260705405710 [Unit of Use] |
HIBCC | D89260705405711 [Primary] |
HIBCC | D89260705405712 [Package] Contains: D89260705405711 Package: Case [4000 Units] In Commercial Distribution |
EJR | Agent, Polishing, Abrasive, Oral Cavity |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-10-28 |
Device Publish Date | 2022-10-20 |
D89260705405852 | 6070540585 |
D89260705405812 | 6070540581 |
D89260705405762 | 6070540576 |
D89260705405752 | 6070540575 |
D89260705405722 | 6070540572 |
D89260705405712 | 6070540571 |
D89260705405662 | 6070540566 |
D89260705405652 | 6070540565 |
D89260705405622 | 6070540562 |
D89260705405612 | 6070540561 |
D89260705405602 | 6070540560 |
D89260705405502 | 6070540550 |