EVIS EXERA ¿ COLONOVIDEOSCOPE

GUDID 04953170202537

OLYMPUS MEDICAL SYSTEMS CORP.

Flexible video colonoscope, reusable

• Primary Device ID: 04953170202537
• NIH Device Record Key: fcc518a4-97e7-4c7a-8ce9-05f575e6a6cd
• Commercial Distribution Discontinuation: 2018-08-09
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: EVIS EXERA ¿ COLONOVIDEOSCOPE
• Version Model Number: CF-Q165I
• Company DUNS: 711789789
• Company Name: OLYMPUS MEDICAL SYSTEMS CORP.
• Device Count: 1
• DM Exempt: false
• 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	04953170202537 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K001241

FDA Product Code

• FDF: Colonoscope and accessories, flexible/rigid

Sterilization

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

[04953170202537]

Ethylene Oxide;High-level Disinfectant

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-08-10
• Device Publish Date: 2016-09-21

On-Brand Devices [EVIS EXERA ¿ COLONOVIDEOSCOPE]

• 04953170339691: CF-Q165L
• 04953170339684: CF-Q165I
• 04953170202537: CF-Q165I
• 04953170202476: CF-Q165L