Primary Device ID | 10850012846229 |
NIH Device Record Key | 2a2ac0f3-b44d-4ad0-95fd-875e7469e93b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | JNW URTRAC™ |
Version Model Number | 081300 |
Catalog Number | 081300 |
Company DUNS | 603420183 |
Company Name | LSI Solutions, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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(866)575-3493 |
regulatorydpt@lsisolutions.com | |
Phone | +1(866)575-3493 |
regulatorydpt@lsisolutions.com | |
Phone | +1(866)575-3493 |
regulatorydpt@lsisolutions.com | |
Phone | +1(866)575-3493 |
regulatorydpt@lsisolutions.com | |
Phone | +1(866)575-3493 |
regulatorydpt@lsisolutions.com | |
Phone | +1(866)575-3493 |
regulatorydpt@lsisolutions.com | |
Phone | +1(866)575-3493 |
regulatorydpt@lsisolutions.com | |
Phone | +1(866)575-3493 |
regulatorydpt@lsisolutions.com | |
Phone | +1(866)575-3493 |
regulatorydpt@lsisolutions.com | |
Phone | +1(866)575-3493 |
regulatorydpt@lsisolutions.com | |
Phone | +1(866)575-3493 |
regulatorydpt@lsisolutions.com | |
Phone | +1(866)575-3493 |
regulatorydpt@lsisolutions.com | |
Phone | +1(866)575-3493 |
regulatorydpt@lsisolutions.com | |
Phone | +1(866)575-3493 |
regulatorydpt@lsisolutions.com | |
Phone | +1(866)575-3493 |
regulatorydpt@lsisolutions.com | |
Phone | +1(866)575-3493 |
regulatorydpt@lsisolutions.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850012846222 [Primary] |
GS1 | 10850012846229 [Package] Contains: 00850012846222 Package: Case [6 Units] In Commercial Distribution |
GEA | CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-03-15 |
Device Publish Date | 2022-03-07 |
10850012846342 - RAPORT™ | 2024-05-30 RAPORT™ KIT |
10850012846335 - PROSTAGRIP™ | 2024-04-29 PROSTAGRIP™ DEVICE |
10850012846281 - VIRTUOSEW™ | 2024-02-22 VIRTUOSEW™ DEVICE |
10850012846298 - AVR NAVIGATOR™ | 2024-02-12 AVR NAVIGATOR™ SMALL RETRACTOR WITH DELIVERY DEVICE |
10850012846304 - AVR NAVIGATOR™ | 2024-02-12 AVR NAVIGATOR™ MEDIUM RETRACTOR WITH DELIVERY DEVICE |
10850012846311 - AVR NAVIGATOR™ | 2024-02-12 AVR NAVIGATOR™ LARGE RETRACTOR WITH DELIVERY DEVICE |
00850012846321 - miniARM® multiSTATION™ System | 2024-01-11 BITA RetroSterno™ Paddle |
10850012846267 - AnastoPod™ | 2023-07-31 AnastoPod™ DEVICE |