Primary Device ID | 08806145475886 |
NIH Device Record Key | cde05250-9567-47de-9cef-4c5799fa217f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Abso Answer |
Version Model Number | AA-22-345 |
Company DUNS | 688355973 |
Company Name | DENTOS Inc. |
Device Count | 1 |
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 | 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 | 08806145475886 [Primary] |
EJF | Bracket, Metal, Orthodontic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-11-09 |
Device Publish Date | 2020-10-30 |
08806145476173 | AA-18-22 |
08806145476166 | AA-18-21 |
08806145476159 | AA-18-17H |
08806145476142 | AA-18-16H |
08806145476135 | AA-18-U45 |
08806145476128 | AA-18-13H |
08806145476111 | AA-18-12 |
08806145476104 | AA-18-11 |
08806145475947 | AA-22-47H |
08806145475930 | AA-22-46H |
08806145475923 | AA-22-445 |
08806145475916 | AA-22-37H |
08806145475909 | AA-22-36HH |
08806145475893 | AA-22-36H |
08806145475886 | AA-22-345 |
08806145475862 | AA-22-27H |
08806145475855 | AA-22-26H |
08806145475848 | AA-22-22 |
08806145475831 | AA-22-21 |
08806145475824 | AA-22-17H |
08806145475817 | AA-22-16H |
08806145475800 | AA-22-U45 |
08806145475794 | AA-22-12 |
08806145475787 | AA-22-11 |
08806145475770 | AA-22-43H |
08806145475763 | AA-22-33H |
08806145475756 | AA-22-23H |
08806145475749 | AA-22-13H |
08806145475732 | AA-22-46HH |