Primary Device ID | 06973456940661 |
NIH Device Record Key | 9f21dc89-a276-45c2-bc12-7f2b923c0c4d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PUSEN |
Version Model Number | RS008-11194 |
Catalog Number | 10.01.0008.00 |
Company DUNS | 543045577 |
Company Name | CORITON Instrument 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 | true |
Serial Number | false |
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 |
Phone | +18475621702 |
info@coriton.com | |
Phone | +18475621702 |
info@coriton.com | |
Phone | +18475621702 |
info@coriton.com | |
Phone | +18475621702 |
info@coriton.com | |
Phone | +18475621702 |
info@coriton.com | |
Phone | +18475621702 |
info@coriton.com | |
Phone | +18475621702 |
info@coriton.com | |
Phone | +18475621702 |
info@coriton.com | |
Phone | +18475621702 |
info@coriton.com | |
Phone | +18475621702 |
info@coriton.com | |
Phone | +18475621702 |
info@coriton.com | |
Phone | +18475621702 |
info@coriton.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06973456940661 [Primary] |
FOX | Stand, Infusion |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-02-27 |
Device Publish Date | 2025-02-19 |
06973456940654 | Trolley |
06973456940661 | Trolley |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() PUSEN 79229017 5548053 Live/Registered |
Zhuhai Pusen Medical Technology Co., Ltd. 2018-01-24 |