Primary Device ID | 08800053083829 |
NIH Device Record Key | 40ccf749-68fc-4e40-b3cb-63b88258364b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LUVIS-C200 Series |
Version Model Number | C200 HEAD |
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 | 08800053083829 [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 |
08800053084024 | AC 100-240 V, 1.5 A, 50-60 Hz |
08800053084017 | AC 100-240 V, 1.5 A, 50-60 Hz |
08800053084000 | AC 12-18 V, 2.0 A, 50/60 Hz AC 100-240 V, 1.5 A, 50-60 Hz |
08800053083997 | AC 12-18 V, 2.0 A, 50/60 Hz |
08800053083850 | AC 100-240 V 1.5 A, 50-60 Hz |
08800053083843 | AC 100-240 V 1.5 A, 50-60 Hz |
08800053083836 | AC 12-18 V, 2.0 A, 50/60 Hz AC 100-240 V 1.5 A, 50-60 Hz |
08800053083829 | AC 12-18 V, 2.0 A, 50/60 Hz |