Portex

Primary DI
35019517046186
Brand
Portex
Company
SMITHS MEDICAL MD, INC.
Model
101/506/030
Published
2018-03-21
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
MR Safe
Rx
true
OTC
false
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
JOHTube tracheostomy and tube cuff

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
JOHTube Tracheostomy And Tube CuffAnesthesiology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K170720000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K170720000Portex Blue Line Ultra Paediatric Tracheosomy TubeSmiths Medical Asd, Inc.2017-12-07JOH

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
35019517046186PackageGS110In Commercial Distribution
55019517046180PackageGS110In Commercial Distribution
15019517046182PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized table
Source identifierGTIN-14 normalized
3501951704618635019517046186
5501951704618055019517046180
1501951704618215019517046182

GMDN Terms#

Term, Definition table
TermDefinition
Basic tracheostomy tube, single-useA sterile hollow cylinder designed to be inserted into an artificial opening made in the trachea (windpipe) during a tracheotomy to provide a patent airway. It is typically constructed of plastic and may include an inner cannula. It is available in cuffed, uncuffed, and/or fenestrated versions, and in a variety of shapes and sizes to meet the individual needs of the patient. It is typically secured in position by a tracheostomy tube holder fastened around the patient's neck. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Circumference3Millimeter
Device Size Text, specify0

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
106712748
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
true
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
30610586043325Level 1SWU-20012016-10-11
30610586043332Level 1SWU-20022016-10-11
30610586043349Level 1SWU-20032016-10-11
30610586043356Level 1SWU-20042016-10-11
30610586043363Level 1SWU-20072016-10-11
30610586043387Level 1SWU-20092016-10-11
30610586043394Level 1SWU-20102016-10-11
30610586043400Level 1SWU-20112016-10-11
30610586043417Level 1SWU-20132016-10-11
30610586043424Level 1SWU-2014L2016-10-11
30610586043431Level 1SWU-2014R2016-10-11
30610586043448Level 1SWU-20162016-10-11
30610586043455Level 1SWU-20182016-10-11
30610586043479Level 1SWU-21132016-10-11
30695085002769Level 1SW-2014L2016-10-11
30695085002776Level 1SW-2014R2016-10-11
30351688428350Portex0082012021-02-23
30610586016534Deltec21-2905-012015-09-01
30610586025635Deltec21-2770-242017-01-24
30610586025659Deltec21-2861-242016-10-13

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Primary DI, Brand, Company table
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