| Primary Device ID | 26974481831171 |
| NIH Device Record Key | a34c978a-4e3e-4b3b-8b8a-70530eef87e8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | IMPROSAFE® Multi Sample Needle |
| Version Model Number | 22G×1 1/2” |
| Catalog Number | 598122380 |
| Company DUNS | 554555378 |
| Company Name | Guangzhou Improve Medical Instruments 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 | true |
| 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 | 06974481831177 [Primary] |
| GS1 | 26974481831171 [Package] Contains: 06974481831177 Package: [25 Units] In Commercial Distribution |
| GS1 | 66974481831179 [Package] Package: 8(25*8) [200 Units] In Commercial Distribution |
| FMI | Needle, Hypodermic, Single Lumen |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-03-24 |
| Device Publish Date | 2025-03-14 |
| 56933395620838 | 22G × 1 1/2″ |
| 56933395620821 | 22G × 1″ |
| 56933395620814 | 21G × 1 1/2″ |
| 56933395620807 | 21G × 1″ |
| 56933395620791 | 22G × 1 1/2″ |
| 56933395620784 | 22G × 1″ |
| 56933395620777 | 21G × 1 1/2″ |
| 56933395620760 | 21G × 1″ |
| 56933395620753 | 22G × 1 1/2″ |
| 56933395620746 | 22G × 1″ |
| 56933395620739 | 21G × 1 1/2″ |
| 56933395620722 | 21G × 1″ |
| 26974481831171 | 22G×1 1/2” |
| 26974481831157 | 22G×1” |
| 26974481831133 | 21G×1 1/2” |
| 26974481831119 | 21G×1” |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() IMPROSAFE 97623726 not registered Live/Pending |
GIMDx, Inc 2022-10-07 |
![]() IMPROSAFE 86636308 not registered Dead/Abandoned |
GIMDX, INC. 2015-05-20 |