Vapor Line Reusable Process Challenge Device 26906900

GUDID 30818087010994

Vapor Line Reusable Process Challenge Device

PROPPER MANUFACTURING COMPANY, INC.

Chemical/physical sterilization process indicator
Primary Device ID30818087010994
NIH Device Record Key1190a20d-b4dd-4497-b2e6-c4a6528870e7
Commercial Distribution StatusIn Commercial Distribution
Brand NameVapor Line Reusable Process Challenge Device
Version Model Number26906900
Catalog Number26906900
Company DUNS001483130
Company NamePROPPER MANUFACTURING COMPANY, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS130818087010994 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JOJIndicator, Physical/Chemical Sterilization Process

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-06-26
Device Publish Date2023-06-16

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