RECORDER UNIT N2483440

GUDID 04953170244506

OLYMPUS MEDICAL SYSTEMS CORP.

Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor Video capsule endoscopy system monitor
Primary Device ID04953170244506
NIH Device Record Key727a19ca-0cbf-4dd9-b739-6d2e309a2e10
Commercial Distribution StatusIn Commercial Distribution
Brand NameRECORDER UNIT
Version Model NumberOLYMPUS RE-1
Catalog NumberN2483440
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 Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
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

Device Identifiers

Device Issuing AgencyDevice ID
GS104953170244506 [Primary]

FDA Product Code

NEZSystem, Imaging, Gastrointestinal, Wireless, Capsule

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-06-29
Device Publish Date2023-06-21

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