SUCTION CLEANING AD

GUDID 04953170071386

OLYMPUS MEDICAL SYSTEMS CORP.

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 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

Primary Device ID	04953170071386
NIH Device Record Key	d53c972d-c2a7-422d-b50d-df82e13e5d85
Commercial Distribution Status	In Commercial Distribution
Brand Name	SUCTION CLEANING AD
Version Model Number	MAJ-222
Company DUNS	711789789
Company Name	OLYMPUS MEDICAL SYSTEMS CORP.
Device Count	1
DM Exempt	true
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	true
Serial Number	false
Manufacturing Date	true
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	false

Customer Support Contacts

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04953170071386 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K201300
Premarket Notification: K963033

FDA Product Code

EOQ	Bronchoscope (Flexible Or Rigid)