Pro-Nox Medium Disposable Kit PROMEDKIT

GUDID 10889483231715

PROMEDKIT, Pro-Nox Medium Disposable Kit, Patient Circuit, 77' Magenta Tubing, Medium Mask

SUNMED, LLC

Anaesthesia breathing circuit, single-use
Primary Device ID10889483231715
NIH Device Record Keybfbc567d-a46e-4284-a69e-db30443f9cdf
Commercial Distribution StatusIn Commercial Distribution
Brand NamePro-Nox Medium Disposable Kit
Version Model NumberPROMEDKIT
Catalog NumberPROMEDKIT
Company DUNS069009268
Company NameSUNMED, LLC
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-800-433-2797
Emailinfo@sun-med.com
Phone1-800-433-2797
Emailinfo@sun-med.com
Phone1-800-433-2797
Emailinfo@sun-med.com
Phone1-800-433-2797
Emailinfo@sun-med.com
Phone1-800-433-2797
Emailinfo@sun-med.com
Phone1-800-433-2797
Emailinfo@sun-med.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100709078006715 [Previous]
GS110889483231715 [Primary]
GS120889483231712 [Package]
Package: Box [20 Units]
In Commercial Distribution

FDA Product Code

CAHFilter, Bacterial, Breathing-Circuit

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-12-23
Device Publish Date2025-12-15

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