Primary Device ID | 50382903057790 |
NIH Device Record Key | 5dfafc24-8d3d-4a44-895d-2aeff7476459 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BD Luer-Lok, BD Eclipse |
Version Model Number | 305779 |
Catalog Number | 305779 |
Company DUNS | 001292192 |
Company Name | BECTON, DICKINSON AND COMPANY |
Device Count | 50 |
DM Exempt | true |
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 | 00382903057795 [Unit of Use] |
GS1 | 30382903057796 [Primary] |
GS1 | 50382903057790 [Package] Contains: 30382903057796 Package: Case [6 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 | 2018-09-12 |
Device Publish Date | 2016-09-16 |
50382903057899 | SYRINGE 1ML LL W/NDL ECLIPSE 27X1/2 RB |
50382903057882 | SYRINGE 3ML LL W/NDL ECLIPSE 22X1 RB |
50382903057875 | SYRINGE 3ML LL W/NDL ECLIPSE 25X1 RB |
50382903057868 | SYR 10ML LL W/NDL ECLIPSE 22X1-1/2 RB |
50382903057851 | Syringe 5ml LL w/Needle 22x1-1/2in RB |
50382903057844 | SYR 3ML LL W/NDL ECLIPSE 21X1-1/2 RB TW |
50382903057837 | SYRINGE 3ML LL W/NDL ECLIPSE 22X1-1/2 RB |
50382903057820 | SYRINGE 3ML LL W/NDL ECLIPSE 23X1 RB |
50382903057813 | SYRINGE 3ML LL W/NDL ECLIPSE 25X5/8 RB |
50382903057806 | SYRINGE 1ML LL W/NDL ECLIPSE 25X5/8 RB |
50382903057790 | SYRINGE 3ML LL W/NDL ECLIPSE 21X1 RB |
50382903057783 | SYRINGE 1ML LL W/NDL ECLIPSE 30x1/2 RB |