Manifold 193145
GUDID 20886333207125
2 Port Manifold w/6" Ext. Right/On/Finger Grip - 200 PSI
ARGON MEDICAL DEVICES, INC.
Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose| Primary Device ID | 20886333207125 |
| NIH Device Record Key | f2cf6cb8-e405-4b2c-a814-1a293902c0c7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Manifold |
| Version Model Number | 193145 |
| Catalog Number | 193145 |
| Company DUNS | 140727624 |
| Company Name | ARGON MEDICAL DEVICES, 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 | true |
| 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 |
Customer Support Contacts
Device Dimensions
| 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 Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00886333207121 [Primary] |
| GS1 | 20886333207125 [Package] Contains: 00886333207121 Package: Box [25 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K915301
FDA Product Code
| DTL | Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-09 |
On-Brand Devices [Manifold]
| 20886333219685 | 3 Port Manifold - Los Alamitos General Hospital |
| 20886333207156 | 4 Port Manifold Left/Off/Finger Grip - 500 PSI |
| 20886333207132 | 2 Port Manifold w/6" Ext. Right/Off/Finger Grip - 200 PSI |
| 20886333207125 | 2 Port Manifold w/6" Ext. Right/On/Finger Grip - 200 PSI |
| 20886333207095 | 4 Port Manifold - Right/Off/Open Body - 500 PSI |
| 20886333207088 | 4 Port Manifold - Right/On/Open Body - 500 PSI |
| 20886333207071 | 3 Port Manifold - Left/Off/Block Body - 500 PSI |
| 20886333207064 | 3 Port Manifold - Right/Off/Block Body - 500 PSI |
| 20886333207057 | 3 Port Manifold - Right/On/Finger Grip - 500 PSI |
| 20886333207033 | 3 Port Manifold - Right/Off/Open Body - 500 PSI |
| 20886333207019 | 2 Port Manifold - Left/Off/Block Body - 500 PSI |
| 20886333207002 | 2 Port Manifold - Right/Off/Block Body - 500 PSI |
| 20886333206982 | 2 Port Manifold - Left/Off/Open Body - 500 PSI |
| 20886333206975 | 2 Port Manifold - Right/Off/Open Body - 500 PSI |
| 20886333206968 | 2 Port Manifold - Right/On/Open Body - 500 PSI |
| 20886333202618 | Manifold 5 Unit w/ Lt. Male Adapter |
Trademark Results [Manifold]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MANIFOLD 97654961 not registered Live/Pending |
Rosen's, Inc. 2022-10-31 |
 MANIFOLD 97085914 not registered Live/Pending |
Adaptive Sensory Technology, Inc. 2021-10-21 |
 MANIFOLD 88125327 not registered Live/Pending |
Red.com, LLC 2018-09-20 |
 MANIFOLD 88000660 not registered Live/Pending |
Arigato Machine Inc. 2018-06-14 |
 MANIFOLD 88000620 not registered Live/Pending |
Arigato Machine Inc. 2018-06-14 |
 MANIFOLD 87872454 not registered Live/Pending |
Manifold Inc. 2018-04-11 |
 MANIFOLD 87857775 not registered Live/Pending |
Adaptive Sensory Technology, Inc. 2018-03-30 |
 MANIFOLD 86752154 5360421 Live/Registered |
SZ DJI Technology Co., Ltd. 2015-09-09 |
 MANIFOLD 86128314 4800387 Live/Registered |
Kai U.S.A., Ltd. 2013-11-25 |
 MANIFOLD 79129490 4423671 Live/Registered |
OKAMURA CORPORATION 2013-03-22 |
 MANIFOLD 78521723 3045772 Live/Registered |
MANIFOLD SOFTWARE LIMITED 2004-11-23 |
 MANIFOLD 78170905 not registered Dead/Abandoned |
Alexander, Todd A., 2002-10-04 |
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