Propper Miller Fiber Optic Laryngoscope Blade #2 19925800

GUDID 30818087011458

Propper Miller Fiber Optic Laryngoscope Blade #2

PROPPER MANUFACTURING COMPANY, INC.

Rigid intubation laryngoscope, reusable
Primary Device ID30818087011458
NIH Device Record Key9436ca5c-381e-4451-b236-4bd31a7a721c
Commercial Distribution StatusIn Commercial Distribution
Brand NamePropper Miller Fiber Optic Laryngoscope Blade #2
Version Model Number19925800
Catalog Number19925800
Company DUNS001483130
Company NamePROPPER MANUFACTURING COMPANY, 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 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
GS130818087011458 [Primary]

FDA Product Code

CCWLaryngoscope, Rigid

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[30818087011458]

Ethylene Oxide;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-03-12
Device Publish Date2020-03-04

On-Brand Devices [Propper Miller Fiber Optic Laryngoscope Blade #2]

30818087011458Propper Miller Fiber Optic Laryngoscope Blade #2
30818087011137Propper Miller Fiber Optic Laryngoscope Blade #2

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.