Primary Device ID | 20813079020121 |
NIH Device Record Key | 2bf3f2b1-a3dd-491d-8640-fe81e15cd78a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Luer Loc Standard Syringe |
Version Model Number | LLS-10-W |
Catalog Number | LLS-10-W |
Company DUNS | 788472314 |
Company Name | REMINGTON MEDICAL, INC. |
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 | true |
OTC Over-The-Counter | false |
Phone | +1(800)989-0057 |
Quality@Remmed.com | |
Phone | +1(800)989-0057 |
Quality@Remmed.com |
Total Volume | 10 Milliliter |
Total Volume | 10 Milliliter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00813079020127 [Primary] |
GS1 | 10813079020124 [Package] Contains: 00813079020127 Package: Inner Carton [25 Units] In Commercial Distribution |
GS1 | 20813079020121 [Package] Contains: 10813079020124 Package: Shipping Carton [10 Units] In Commercial Distribution |
FMF | Syringe, piston |
Steralize Prior To Use | true |
Device Is Sterile | true |
[20813079020121]
Ethylene Oxide
[20813079020121]
Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-09-12 |
Device Publish Date | 2016-09-21 |
20813079020121 | 10cc (White) |
20813079020114 | 10cc (Light Green) |
10813079020100 | 10cc (Green) |
10813079020094 | 10cc (Yellow) |
10813079020087 | 10cc (Blue) |
10813079020070 | 10cc (Red) |