| Primary Device ID | 30351688009283 |
| NIH Device Record Key | 914297f9-77c8-4d83-9524-2c0390217a42 |
| Commercial Distribution Discontinuation | 2015-10-23 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Portex |
| Version Model Number | 555050 |
| Company DUNS | 215591523 |
| Company Name | Smiths Medical International Ltd |
| 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 30351688009283 [Primary] |
| BTO | Tube, tracheostomy (w/wo connector) |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2015-10-21 |
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 |