Primary Device ID | 06970401810826 |
NIH Device Record Key | 90f8da92-eb2d-430e-8979-b45a254732b0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Single Use Cytology Brush |
Version Model Number | MD-L-CB-2823-3010 |
Company DUNS | 544434963 |
Company Name | Zhejiang Chuangxiang Medical Technology Co., LTD. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
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 | 06970401810826 [Primary] |
FDX | Endoscopic Cytology Brush |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-05-26 |
Device Publish Date | 2023-05-18 |
06970401810895 | MD-U-CB-3723-6008 |
06970401810888 | MD-U-CB-2820-6008 |
06970401810871 | MD-U-CB-2016-4008 |
06970401810864 | MD-U-CB-2012-4008 |
06970401810857 | MD-L-CB-3723-5010 |
06970401810840 | MD-L-CB-3720-5010 |
06970401810833 | MD-L-CB-3716-5010 |
06970401810826 | MD-L-CB-2823-3010 |
06970401810819 | MD-L-CB-2820-3010 |
06970401810802 | MD-L-CB-2816-3010 |
06970401810796 | MD-L-CB-2023-2010 |
06970401810789 | MD-L-CB-2020-2010 |
06970401810772 | MD-L-CB-2016-2010 |
06970401810765 | MD-L-CB-2012-5010 |
06970401810758 | MD-L-CB-2012-3010 |
06970401810741 | MD-L-CB-2012-2010 |
06970401810734 | MD-L-CB-2012-1210 |
06970401810727 | MD-L-CB-2007-2010 |
06970401810710 | MD-L-CB-1212-2006 |
06970401810703 | MD-L-CB-1210-1006 |
06970401810697 | MD-L-CB-1207-1006 |