Primary Device ID | 08800053064125 |
NIH Device Record Key | d49ccfe7-a096-4913-88cb-bf44d100405b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | M210 Series (Ceiling, Mobile) |
Version Model Number | M210 |
Company DUNS | 694721181 |
Company Name | DENTIS CO. ,LTD |
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 | true |
Manufacturing Date | true |
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 | 08800053064125 [Primary] |
FTD | Lamp, Surgical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-01-31 |
Device Publish Date | 2024-01-23 |
08800053070553 - s-Clean ScanHealing Abutment Screw | 2024-08-08 s-Clean ScanHealing Abutment Screw (DSSHSM03O) |
08800053070560 - s-Clean ScanHealing Abutment Screw | 2024-08-08 s-Clean ScanHealing Abutment Screw (DSSHSM04O) |
08800053070577 - s-Clean ScanHealing Abutment Screw | 2024-08-08 s-Clean ScanHealing Abutment Screw (DSSHSM05O) |
08800053070584 - s-Clean ScanHealing Abutment Screw | 2024-08-08 s-Clean ScanHealing Abutment Screw (DSSHSM06O) |
08800053070591 - s-Clean ScanHealing Abutment Screw | 2024-08-08 s-Clean ScanHealing Abutment Screw (DSSHSM07O) |
08800053070706 - s-Clean ScanHealing Abutment | 2024-08-08 s-Clean ScanHealing Abutment (DSSH4820S) |
08800053070713 - s-Clean ScanHealing Abutment | 2024-08-08 s-Clean ScanHealing Abutment (DSSH4830S) |
08800053070720 - s-Clean ScanHealing Abutment | 2024-08-08 s-Clean ScanHealing Abutment (DSSH4840S) |