White cap set

GUDID 04953170026553

"MAJ-941 WHITE CAP SET"

OLYMPUS MEDICAL SYSTEMS CORP.

Endoscopic device sterilization/disinfection tubing set Luminal device flushing tubing set, reusable Luminal device flushing tubing set, reusable Luminal device flushing tubing set, reusable Luminal device flushing tubing set, reusable Luminal device flushing tubing set, reusable Luminal device flushing tubing set, reusable Luminal device flushing tubing set, reusable Luminal device flushing tubing set, reusable Luminal device flushing tubing set, reusable Luminal device flushing tubing set, reusable Luminal device flushing tubing set, reusable Luminal device flushing tubing set, reusable Luminal device flushing tubing set, reusable Luminal device flushing tubing set, reusable Luminal device flushing tubing set, reusable Luminal device flushing tubing set, reusable Endoscope calibration cover, reusable Endoscope calibration cover, reusable Endoscope calibration cover, reusable Endoscope calibration cover, reusable Endoscope calibration cover, reusable Endoscope calibration cover, reusable Endoscope calibration cover, reusable Endoscope calibration cover, reusable Endoscope calibration cover, reusable Endoscope calibration cover, reusable Endoscope calibration cover, reusable Endoscope calibration cover, reusable Endoscope calibration cover, reusable Endoscope calibration cover, reusable Endoscope calibration cover, reusable Endoscope calibration cover, reusable
Primary Device ID04953170026553
NIH Device Record Keyce26d941-397f-41cf-a2dd-0084355fa642
Commercial Distribution StatusIn Commercial Distribution
Brand NameWhite cap set
Version Model NumberMAJ-941
Company DUNS711789789
Company NameOLYMPUS MEDICAL SYSTEMS CORP.
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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS104953170026553 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FDSGastroscope and accessories, flexible/rigid

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-11-08
Device Publish Date2016-09-21

On-Brand Devices [White cap set]

04953170027130"MH-154 WHITE CAP SET"
04953170026553"MAJ-941 WHITE CAP SET"

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