Primary Device ID | 08800053045087 |
NIH Device Record Key | 822a68d4-c297-4418-a722-4cb14e42a5d4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LUVIS-C700 Series |
Version Model Number | C700-C0S0A1 |
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 | 08800053045087 [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 |
08800053053853 | AC 12-24 V, 50/60 Hz, 20-21 VA |
08800053053846 | AC 12-24 V, 50/60 Hz, 20-21 VA |
08800053053839 | AC 12-24 V, 50/60 Hz, 20-21 VA |
08800053053822 | AC 12-24 V, 50/60 Hz, 20-21 VA |
08800053045100 | AC 100-240 V, 50-60 Hz, 30-45 VA |
08800053045094 | AC 100-240 V, 50-60 Hz, 30-45 VA |
08800053045087 | AC 100-240 V, 50-60 Hz, 30-45 VA |
08800053045070 | AC 100-240 V, 50-60 Hz, 30-45 VA |