Primary Device ID | 56933395620890 |
NIH Device Record Key | 636baf85-370f-4812-8fd4-a9cc10584fc0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | IMPROSAFE® Multi Sample Needle (Flashback) |
Version Model Number | 21G × 1 1/4″ |
Company DUNS | 530148444 |
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 | 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 | 06933395620895 [Primary] |
GS1 | 16933395620892 [Package] Contains: 06933395620895 Package: [50 Units] In Commercial Distribution |
GS1 | 46933395620893 [Package] Contains: 16933395620892 Package: [10 Units] In Commercial Distribution |
GS1 | 56933395620890 [Package] Contains: 16933395620892 Package: [4 Units] In Commercial Distribution |
FMI | Needle, Hypodermic, Single Lumen |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-01-08 |
Device Publish Date | 2016-12-23 |
56933395620951 | 22G × 1 1/4″ |
56933395620944 | 22G × 1″ |
56933395620937 | 21G × 1 1/4″ |
56933395620920 | 21G × 1″ |
56933395620913 | 22G × 1 1/4″ |
56933395620906 | 22G × 1″ |
56933395620890 | 21G × 1 1/4″ |
56933395620883 | 21G × 1″ |
56933395620876 | 22G × 1 1/4″ |
56933395620869 | 22G × 1″ |
56933395620852 | 21G × 1 1/4″ |
56933395620845 | 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 |