Primary Device ID | 00860010019689 |
NIH Device Record Key | b09e2764-3d94-4108-a83b-8d992afe013e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MirroSoft™ No. 5 Double Mirror |
Version Model Number | 83203 |
Company DUNS | 035988858 |
Company Name | Armor Dental Corp. |
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 | false |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00860010019689 [Primary] |
EAX | Mirror, Mouth |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-05-20 |
Device Publish Date | 2025-05-12 |
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00860010019689 - MirroSoft™ No. 5 Double Mirror | 2025-05-20 |
00860010019689 - MirroSoft™ No. 5 Double Mirror | 2025-05-20 |
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