| Primary Device ID | 16943718223297 |
| NIH Device Record Key | 7609874d-526a-48f4-bc45-46f44e368584 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Demax |
| Version Model Number | DHD30P/OFF |
| 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 | true |
| 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06943718223290 [Primary] |
| GS1 | 16943718223297 [Package] Contains: 06943718223290 Package: [20 Units] In Commercial Distribution |
| MAV | Syringe, Balloon Inflation |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-09-20 |
| Device Publish Date | 2022-09-12 |
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 |