Primary Device ID | 03661540303975 |
NIH Device Record Key | 325889b2-70a2-4263-b295-fb2bd0de7718 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ELITechGroup |
Version Model Number | Model 7622 |
Company DUNS | 052423787 |
Company Name | ELITECHGROUP 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 | false |
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 | 03661540303975 [Primary] |
IFB | Cytocentrifuge |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2021-02-22 |
Device Publish Date | 2016-09-24 |
03661540304088 | The ChloroChek Chloridometer test system is intended for the quantitative in vitro diagnostic de |
03661540303975 | The Cytopro Cytocentrifuge is an in vitro diagnostic medical device for fixing biological cell s |
03661540303951 | Model 7322 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ELITECHGROUP 85927180 4822550 Live/Registered |
Wescor Inc. 2013-05-09 |