Primary Device ID | 04987669101483 |
NIH Device Record Key | 6145b008-df39-402e-bb4a-c60c3fca82ae |
Commercial Distribution Discontinuation | 2019-03-29 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | System Table |
Version Model Number | ST-6100 |
Company DUNS | 690635461 |
Company Name | NIDEK 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 | false |
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 |
Phone | 1-800-223-9044 |
info@nidek.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04987669101483 [Primary] |
HRJ | Table, Instrument, 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 | 2019-04-03 |
Device Publish Date | 2019-03-26 |
04987669100806 | The ST-5100 is the system table on which the NIDEK REFRACTOR RT-5100 is installed. The table all |
04987669101490 | The ST-600 is the system table on which the Nidek Refractor RT-6100, RT-3100, or a manually oper |
04987669101483 | The ST-6100 is the system table on which the Nidek Refractor RT-6100, RT-3100, or a manually ope |