Ultipor™ Anesthesia Breathing Circuit System - Patient Kit VMPKXL

GUDID 30636207315381

Extra-Large Vanilla-Scented Adult Face Mask, Ported Elbow, and Ultipor 25 Filter. Non-Conductive, Disposable.

PALL CORPORATION

Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit Patient-end respiratory anaesthesia kit
Primary Device ID30636207315381
NIH Device Record Key8196a3c1-2b50-478e-b098-31830c95f0cf
Commercial Distribution StatusIn Commercial Distribution
Brand NameUltipor™ Anesthesia Breathing Circuit System - Patient Kit
Version Model NumberVMPKXL
Catalog NumberVMPKXL
Company DUNS002054419
Company NamePALL CORPORATION
Device Count1
DM Exempttrue
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com
Phone+1(800)645-6578
EmailQAMedical@pall.com

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Device Identifiers

Device Issuing AgencyDevice ID
GS100636207315380 [Primary]
GS130636207315381 [Package]
Contains: 00636207315380
Package: case [20 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

CAHFilter, bacterial, breathing-circuit

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-06-29

On-Brand Devices [Ultipor™ Anesthesia Breathing Circuit System - Patient Kit]

30636207315381Extra-Large Vanilla-Scented Adult Face Mask, Ported Elbow, and Ultipor 25 Filter. Non-Conductive
30636207315312Large Vanilla-Scented Adult Face Mask, Ported Elbow, and Ultipor 25 Filter
30636207315305Medium Vanilla-Scented Adult Face Mask, Ported Elbow, and Ultipor 25 Filter. Non-Conductive, Dis
30636207315299Small Vanilla-Scented Adult Face Mask, Ported Elbow and Ultipor 25 Filter. Non-Conductive, Dispo

Trademark Results [Ultipor]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ULTIPOR
ULTIPOR
72140583 0746229 Live/Registered
PALL CORPORATION
1962-03-23

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