Primary Device ID | 08800053053808 |
NIH Device Record Key | 478ca773-c117-4225-b3e5-07e1f46f3986 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LUVIS-C600 Series |
Version Model Number | C600-W0S0A0 |
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 | 08800053053808 [Primary] |
EAZ | Light, Operating, 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 | 2024-01-31 |
Device Publish Date | 2024-01-23 |
08800053053815 | AC 12-24 V, 50/60 Hz, 20-21 VA |
08800053053808 | AC 12-24 V, 50/60 Hz, 20-21 VA |
08800053053792 | AC 12-24 V, 50/60 Hz, 20-21 VA |
08800053053785 | AC 12-24 V, 50/60 Hz, 20-21 VA |
08800053045063 | AC 100-240 V, 50-60 Hz, 30-45 VA |
08800053045056 | AC 100-240 V, 50-60 Hz, 30-45 VA |
08800053045049 | AC 100-240 V, 50-60 Hz, 30-45 VA |
08800053045032 | AC 100-240 V, 50-60 Hz, 30-45 VA |