Primary Device ID | 04580606431836 |
NIH Device Record Key | 1d1580fc-52b7-41ff-8070-d2b799354a07 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Visionix |
Version Model Number | Retinomax Screeen |
Catalog Number | VSN5300TB |
Company DUNS | 713383495 |
Company Name | RIGHT MFG. 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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04580606431836 [Primary] |
HKO | Refractometer, 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 | 2023-01-13 |
Device Publish Date | 2023-01-05 |
04580606431850 | Bear Chart SET |
04580606431843 | Fireworks Chart SET |
04580606431836 | Tulip Chart SET |
04580606431768 | Bear Chart SET |
04580606431751 | Fireworks Chart SET |
04580606431744 | Tulip Chart SET |
04580606431652 | Tulip Chart SET |
04580606431584 | DIGITAL PHOTO UNIT SET |
04580606431553 | DIGITAL PHOTO UNIT SET |
04580606431522 | CLINICAL UNIT SET |
04580606431492 | CLINICAL UNIT SET |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VISIONIX 97162724 not registered Live/Pending |
Luneau Technology Operations 2021-12-08 |
VISIONIX 85150220 4015109 Live/Registered |
VISIONIX LTD. 2010-10-12 |
VISIONIX 77374238 4077385 Live/Registered |
THALES DEFENSE & SECURITY, INC. 2008-01-17 |
VISIONIX 75741616 2410211 Dead/Cancelled |
VISIONIX LTD. 1999-06-25 |