Suction Tube

GUDID 04953170026737

"MB-721 SUCTION TUBE FOR LUS"

OLYMPUS MEDICAL SYSTEMS CORP.

Endoscopic procedure air/water valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable
Primary Device ID04953170026737
NIH Device Record Keyaba77fd9-a500-42fd-aafe-c9c36e3b2997
Commercial Distribution StatusIn Commercial Distribution
Brand NameSuction Tube
Version Model NumberMB-721
Company DUNS711789789
Company NameOLYMPUS MEDICAL SYSTEMS CORP.
Device Count1
DM Exempttrue
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
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
GS104953170026737 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FEOLithotriptor, ultrasonic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


[04953170026737]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number6
Public Version Date2018-10-08
Device Publish Date2016-09-21

On-Brand Devices [Suction Tube]

04953170061325REUSABLE SUCTION TUBING FOR UHI
04953170026737"MB-721 SUCTION TUBE FOR LUS"

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