EVIS DUODENOVIDEOSCOPE

GUDID 04953170066344

OLYMPUS MEDICAL SYSTEMS CORP.

Flexible video duodenoscope, reusable

• Primary Device ID: 04953170066344
• NIH Device Record Key: 6aebe6b7-9453-454f-8db6-dbdf9c635ff1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EVIS DUODENOVIDEOSCOPE
• Version Model Number: OLYMPUS JF TYPE 140F
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04953170066344 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K954451

FDA Product Code

• FET: Endoscopic video imaging system/component, gastroenterology-urology

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[04953170066344]

Ethylene Oxide;High-level Disinfectant

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-01-23
• Device Publish Date: 2016-09-21

On-Brand Devices [EVIS DUODENOVIDEOSCOPE]

• 04953170339851: JF-140R
• 04953170339844: JF-140F DUODENOVIDEOSCOPE (FIXED CAP)
• 04953170066344: OLYMPUS JF TYPE 140F