RHINO-LARYNGO FIBERSCOPE

GUDID 04953170318221

OLYMPUS MEDICAL SYSTEMS CORP.

Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope Flexible fibreoptic nasopharyngolaryngoscope

Primary Device ID	04953170318221
NIH Device Record Key	7e145101-213e-4abd-988a-9507d0fcf16b
Commercial Distribution Status	In Commercial Distribution
Brand Name	RHINO-LARYNGO FIBERSCOPE
Version Model Number	OLYMPUS ENF TYPE XP
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	false
Serial Number	true
Manufacturing Date	true
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04953170318221 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K011869

FDA Product Code

EOB	Nasopharyngoscope (flexible or rigid)