Primary Device ID | 26943718281805 |
NIH Device Record Key | 7a662186-19f4-4dd8-b389-39a1458af50d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Demax |
Version Model Number | DQ0623N18 |
Company DUNS | 529725666 |
Company Name | Beijing Demax 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 | 06943718281801 [Primary] |
GS1 | 26943718281805 [Package] Contains: 06943718281801 Package: [30 Units] In Commercial Distribution |
DYB | Introducer, Catheter |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-04-24 |
Device Publish Date | 2023-04-15 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DEMAX 98169204 not registered Live/Pending |
Solnarova Tetiana Victorivna 2023-09-07 |
DEMAX 88232288 not registered Live/Pending |
SATO PHARMACEUTICAL CO., LTD. 2018-12-17 |
DEMAX 87297306 5408740 Live/Registered |
Beijin DeMax Medical TEchnology Co., Ltd. 2017-01-11 |
DEMAX 77821441 not registered Dead/Abandoned |
9150-4084 QUÃBEC INC. 2009-09-08 |
DEMAX 74471213 1873692 Dead/Cancelled |
BRAMWELL, DENTON 1993-12-20 |
DEMAX 74351254 1794959 Dead/Cancelled |
BRAMWELL, DENTON 1993-01-22 |