Primary Device ID | D89260705411282 |
NIH Device Record Key | 3db3ee11-de17-4f6d-9ae5-20abc2f3e50e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | COMBO THREADERS WITH DENTAL FLOSS |
Version Model Number | 6070541128 |
Company DUNS | 079343581 |
Company Name | MAXILL, INC. |
Device Count | 5 |
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 | D89260705411280 [Unit of Use] |
HIBCC | D89260705411281 [Primary] |
HIBCC | D89260705411282 [Package] Contains: D89260705411281 Package: Box [250 Units] In Commercial Distribution |
HIBCC | D89260705411283 [Package] Package: Case [5000 Units] In Commercial Distribution |
JES | Floss, 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 | 2022-09-27 |
Device Publish Date | 2022-09-19 |