Primary Device ID | 50382903057592 |
NIH Device Record Key | 024f5df3-0cf0-4127-aea2-89ab43526967 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BD Eclipse |
Version Model Number | 305759 |
Catalog Number | 305759 |
Company DUNS | 001292192 |
Company Name | BECTON, DICKINSON AND COMPANY |
Device Count | 100 |
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 | 00382903057597 [Unit of Use] |
GS1 | 30382903057598 [Primary] |
GS1 | 50382903057592 [Package] Contains: 30382903057598 Package: Case [12 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 | 5 |
Public Version Date | 2019-10-23 |
Device Publish Date | 2016-09-16 |
50382903057691 | NEEDLE ECLIPSE 23X1-1/4 RB |
50382903057684 | NEEDLE ECLIPSE 22X1 RB |
50382903057677 | NEEDLE ECLIPSE 25X1-1/2 RB |
50382903057660 | NEEDLE ECLIPSE 18X1-1/2 RB |
50382903057653 | NEEDLE ECLIPSE 21X1-1/2 RB TW |
50382903057646 | NEEDLE ECLIPSE 21X1 RB TW |
50382903057639 | NEEDLE ECLIPSE 22X1-1/2 RB |
50382903057622 | NEEDLE ECLIPSE 23X1 RB |
50382903057615 | NEEDLE ECLIPSE 25X1 RB |
50382903057592 | NEEDLE ECLIPSE 25X5/8 |
50382903057585 | NEEDLE ECLIPSE 27X1/2 |
50382903057578 | NEEDLE ECLIPSE 30X1/2 |