Primary Device ID | 35019517115875 |
NIH Device Record Key | 76c1ea4e-2bf7-495f-b116-c2b3e6959519 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Portex |
Version Model Number | NEPI-NLD-49651-27 |
Company DUNS | 137835299 |
Company Name | SMITHS MEDICAL ASD, 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 | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 15019517115871 [Primary] |
GS1 | 35019517115875 [Package] Contains: 15019517115871 Package: CASE [10 Units] In Commercial Distribution |
CAZ | Anesthesia conduction kit |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-07-22 |
Device Publish Date | 2017-08-24 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() PORTEX 88465408 not registered Live/Pending |
XINGUARD INC. 2019-06-09 |
![]() PORTEX 79021653 3253922 Live/Registered |
DESA Tech AG 2006-02-23 |
![]() PORTEX 78236135 2886382 Live/Registered |
SMITHS MEDICAL ASD, INC. 2003-04-10 |
![]() PORTEX 77760408 3780380 Live/Registered |
Smiths Medical ASD, Inc. 2009-06-16 |
![]() PORTEX 75472252 2417963 Dead/Cancelled |
SMITHS MEDICAL ASD, INC. 1998-04-22 |
![]() PORTEX 73833948 1599410 Dead/Cancelled |
PIPER CAPITAL MANAGEMENT INCORPORATED 1989-10-26 |
![]() PORTEX 73475153 1342083 Dead/Cancelled |
Nilsson; Goran Alfred 1984-04-11 |
![]() PORTEX 71516916 0444703 Live/Registered |
PORTLAND PLASTICS LIMITED 1947-02-04 |