Primary Device ID | 14895233608627 |
NIH Device Record Key | 881be704-f699-4112-928c-e341ab464fa6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LCCS |
Version Model Number | ET20113-D-LC |
Company DUNS | 663190222 |
Company Name | LCCS Products Limited |
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 (844) 743-6449 |
info@lccsmedical.com | |
Phone | +1 (844) 743-6449 |
info@lccsmedical.com | |
Phone | +1 (844) 743-6449 |
info@lccsmedical.com | |
Phone | +1 (844) 743-6449 |
info@lccsmedical.com | |
Phone | +1 (844) 743-6449 |
info@lccsmedical.com | |
Phone | +1 (844) 743-6449 |
info@lccsmedical.com | |
Phone | +1 (844) 743-6449 |
info@lccsmedical.com | |
Phone | +1 (844) 743-6449 |
info@lccsmedical.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04895233608620 [Primary] |
GS1 | 14895233608627 [Package] Contains: 04895233608620 Package: Box [25 Units] In Commercial Distribution |
GS1 | 64895233608622 [Package] Package: Carton [40 Units] In Commercial Distribution |
BSP | Needle, Conduction, Anesthetic (W/Wo Introducer) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-08-02 |
Device Publish Date | 2021-07-24 |
64895233608912 | AN-E EPIDURAL NEEDLE |
64895233608745 | AN-E EPIDURAL NEEDLE |
64895233608714 | AN-E EPIDURAL NEEDLE |
64895233608639 | AN-E EPIDURAL NEEDLE |
64895233608615 | AN-E EPIDURAL NEEDLE |
64895233608516 | AN-E EPIDURAL NEEDLE |
64895233608110 | AN-E EPIDURAL NEEDLE |
64895233608011 | AN-E EPIDURAL NEEDLE |
64895233606864 | AN-SI SPINAL NEEDLE |
64895233606710 | AN-SI SPINAL NEEDLE |
64895233606543 | AN-SI SPINAL NEEDLE |
64895233606536 | AN-SI SPINAL NEEDLE |
64895233606529 | AN-SI SPINAL NEEDLE |
64895233606437 | AN-SI SPINAL NEEDLE |
64895233606420 | AN-SI SPINAL NEEDLE |
64895233606246 | AN-SI SPINAL NEEDLE |
64895233606239 | AN-SI SPINAL NEEDLE |
64895233606222 | AN-SI SPINAL NEEDLE |
64895233605249 | LCCS Radiofrequency (RF) Electrode |
64895233605232 | LCCS Radiofrequency (RF) Electrode |
64895233605225 | LCCS Radiofrequency (RF) Electrode |
64895233605218 | LCCS Radiofrequency (RF) Electrode |
64895233605034 | LCCS Radiofrequency (RF) Electrode |
64895233605027 | LCCS Radiofrequency (RF) Electrode |
64895233605010 | LCCS Radiofrequency (RF) Electrode |
64895233602521 | Single-use RF Cannula |
64895233602422 | Single-use RF Cannula |
64895233602323 | Single-use RF Cannula |
64895233602316 | Single-use RF Cannula |
64895233602132 | Single-use RF Cannula |
64895233602026 | Single-use RF Cannula |
64895233601968 | Single-use RF Cannula |
64895233601913 | Single-use RF Cannula |
64895233601838 | Single-use RF Cannula |
64895233601746 | Single-use RF Cannula |
64895233601432 | Single-use RF Cannula |
64895233601326 | Single-use RF Cannula |
64895233601319 | Single-use RF Cannula |
64895233601142 | Single-use RF Cannula |
04895233601027 | Single-use RF Cannula |
14895233608832 | AN-E EPIDURAL NEEDLE |
14895233608825 | AN-E EPIDURAL NEEDLE |
14895233608818 | AN-E EPIDURAL NEEDLE |
14895233608733 | AN-E EPIDURAL NEEDLE |
14895233608726 | AN-E EPIDURAL NEEDLE |
14895233608627 | AN-E EPIDURAL NEEDLE |
14895233608429 | AN-E EPIDURAL NEEDLE |
14895233608412 | AN-E EPIDURAL NEEDLE |
14895233608337 | AN-E EPIDURAL NEEDLE |
14895233608320 | AN-E EPIDURAL NEEDLE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
LCCS 86385291 4853773 Live/Registered |
Ming Lin 2014-09-04 |