Primary Device ID | 30817522012821 |
NIH Device Record Key | 5ace88b0-3bf0-4cc4-aec2-80c0b5e95918 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ameritus |
Version Model Number | ENF-Straw |
Catalog Number | ENF-Straw |
Company DUNS | 066175613 |
Company Name | KENTEC MEDICAL, 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 | 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 |
Phone | 949-863-0810 |
kjrooks@kentecmedical.com | |
Phone | 949-863-0810 |
kjrooks@kentecmedical.com | |
Phone | 949-863-0810 |
kjrooks@kentecmedical.com | |
Phone | 949-863-0810 |
kjrooks@kentecmedical.com | |
Phone | 949-863-0810 |
kjrooks@kentecmedical.com | |
Phone | 949-863-0810 |
kjrooks@kentecmedical.com | |
Phone | 949-863-0810 |
kjrooks@kentecmedical.com | |
Phone | 949-863-0810 |
kjrooks@kentecmedical.com | |
Phone | 949-863-0810 |
kjrooks@kentecmedical.com | |
Phone | 949-863-0810 |
kjrooks@kentecmedical.com | |
Phone | 949-863-0810 |
kjrooks@kentecmedical.com | |
Phone | 949-863-0810 |
kjrooks@kentecmedical.com | |
Phone | 949-863-0810 |
kjrooks@kentecmedical.com | |
Phone | 949-863-0810 |
kjrooks@kentecmedical.com | |
Phone | 949-863-0810 |
kjrooks@kentecmedical.com | |
Phone | 949-863-0810 |
kjrooks@kentecmedical.com | |
Phone | 949-863-0810 |
kjrooks@kentecmedical.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10817522012827 [Primary] |
GS1 | 20817522012824 [Package] Contains: 10817522012827 Package: box [100 Units] In Commercial Distribution |
GS1 | 30817522012821 [Package] Contains: 10817522012827 Package: case [800 Units] In Commercial Distribution |
ILC | Utensil, Eating |
Steralize Prior To Use | true |
Device Is Sterile | true |
[30817522012821]
Ethylene Oxide
[30817522012821]
Ethylene Oxide
[30817522012821]
Ethylene Oxide
[30817522012821]
Ethylene Oxide
[30817522012821]
Ethylene Oxide
[30817522012821]
Ethylene Oxide
[30817522012821]
Ethylene Oxide
[30817522012821]
Ethylene Oxide
[30817522012821]
Ethylene Oxide
[30817522012821]
Ethylene Oxide
[30817522012821]
Ethylene Oxide
[30817522012821]
Ethylene Oxide
[30817522012821]
Ethylene Oxide
[30817522012821]
Ethylene Oxide
[30817522012821]
Ethylene Oxide
[30817522012821]
Ethylene Oxide
[30817522012821]
Ethylene Oxide
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-09-23 |
Device Publish Date | 2019-09-13 |
30817522011305 | 60ml enteral/oral syringe |
30817522011299 | 5ml enteral/oral syringe |
30817522011282 | 3ml enteral/oral syringe |
30817522011275 | 30ml enteral/oral syringe |
30817522011268 | 20ml enteral/oral syringe |
30817522011251 | 1ml enteral/oral syringe |
30817522010001 | 10ml enteral/oral syringe |
30817522012821 | Enfit syringe straw |
30817522010605 | oral syringe straw |
20817522010363 | small size ecg electrode |
20817522010356 | large size ecg electrode |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
AMERITUS 85839780 not registered Dead/Abandoned |
Timex Group USA, Inc. 2013-02-04 |
AMERITUS 85465073 4174712 Live/Registered |
Kentec Medical, Inc. 2011-11-04 |
AMERITUS 76541601 3018292 Live/Registered |
Kentec Medical, Inc. 2003-08-25 |
AMERITUS 76063433 not registered Dead/Abandoned |
HUGHES AIRCRAFT EMPLOYEES FEDERAL CREDIT UNION 2000-06-05 |