Primary Device ID | 00380657530724 |
NIH Device Record Key | e0dc90cf-f1d4-4a2d-9d62-513c7cb47962 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LuxOR Revalia |
Version Model Number | 00380657530724 |
Company DUNS | 008018525 |
Company Name | Alcon Laboratories, Inc. |
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 | 00380657530724 [Primary] |
HRM | MICROSCOPE, OPERATING & ACCESSORIES, AC-POWERED, OPHTHALMIC |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-10-06 |
Device Publish Date | 2022-09-28 |
00380657530731 | Surgical Microscope |
00380657530724 | Surgical Microscope |
00380657530717 | Surgical Microscope |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
LUXOR REVALIA 88195422 not registered Live/Pending |
Alcon Inc. 2018-11-15 |