ULTRASOUND BRONCHOSCOPE

GUDID 04961333232208

LINEAR ULTRASOUND VIDEOBRONCHOSCOPE 2.0C (REFURBISHED)

PENTAX OF AMERICA, INC.

Flexible ultrasound bronchoscope
Primary Device ID04961333232208
NIH Device Record Key2a548897-aaf6-49f4-978d-ccd0f1f33ff1
Commercial Distribution StatusIn Commercial Distribution
Brand NameULTRASOUND BRONCHOSCOPE
Version Model NumberEB-1970UK
Company DUNS083211284
Company NamePENTAX OF AMERICA, 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 Batchfalse
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
GS104961333232208 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

EOQBronchoscope (Flexible Or Rigid)

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04961333232208]

Ethylene Oxide;High-level Disinfectant


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2017-04-06

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