Primary Device ID | 00817617021959 |
NIH Device Record Key | d10873b8-c22e-4841-a72e-e6fa799c5047 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Curaplex |
Version Model Number | 1612-84150 |
Company DUNS | 070556204 |
Company Name | BOUND TREE MEDICAL, LLC |
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 | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Needle Gauge | 22 Gauge |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817617021492 [Package] Contains: 00817617022390 Package: [50 Units] In Commercial Distribution |
GS1 | 00817617021959 [Package] Contains: 00817617021492 Package: [4 Units] In Commercial Distribution |
GS1 | 00817617022390 [Primary] |
FOZ | Catheter,intravascular,therapeutic,short-term less than 30 days |
Steralize Prior To Use | true |
Device Is Sterile | true |
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
[00817617021959]
Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-02-06 |
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00812277033014 | *CUSTOM* South Metro Introcan IV Catheter 16ga |
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00812277032000 | ClearPath Bypass HME |
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00812277031966 | Stop The Bleed Basic Kit- *EMP FOR AMAZON ONLY* |
00812277031959 | *CUSTOM* Shelby Co Blood Draw Kit |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() CURAPLEX 90762116 not registered Live/Pending |
Salient Labs 2021-06-08 |
![]() CURAPLEX 90314879 not registered Live/Pending |
Sarnova HC, LLC 2020-11-12 |
![]() CURAPLEX 85132351 4053956 Live/Registered |
Sarnova HC, LLC 2010-09-17 |
![]() CURAPLEX 72168698 0762640 Dead/Expired |
CHEMWAY CORPORATION 1963-05-13 |