Portex

GUDID 35019315050774

Reinforced endotracheal tube, single-use

Primary Device ID	35019315050774
NIH Device Record Key	d583894c-0edb-4d32-bad5-a0ddc10ed781
Commercial Distribution Status	In Commercial Distribution
Brand Name	Portex
Version Model Number	100/110/065
Company DUNS	215591523
Company Name	Smiths Medical International Ltd
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

Device Issuing Agency	Device ID
GS1	15019315050770 [Primary]
GS1	35019315050774 [Package] Contains: 15019315050770 Package: BOX [5 Units] In Commercial Distribution
GS1	55019315050778 [Package] Package: CASE [10 Units] In Commercial Distribution

BTR	Tube, tracheal (w/wo connector)

Steralize Prior To Use	false
Device Is Sterile	true

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