AED

GUDID 00848657022446

Sinus Suction Tube #501.32

NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.

ENT surgical procedure kit, non-medicated, reusable
Primary Device ID00848657022446
NIH Device Record Key500f9b4b-d434-4178-a579-75c992505d0c
Commercial Distribution StatusIn Commercial Distribution
Brand NameAED
Version Model Number501.32
Company DUNS839138955
Company NameNATIONAL ADVANCED ENDOSCOPY DEVICES, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100848657022446 [Primary]

FDA Product Code

KARIRRIGATOR, SINUS

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00848657022446]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2017-11-20

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