OES EYEPIECE HOOD

GUDID 04953170063954

"MB-326 EYECUP F/OES FIBERSCOPE"

OLYMPUS MEDICAL SYSTEMS CORP.

Endoscope hood

• Primary Device ID: 04953170063954
• NIH Device Record Key: d38529b3-02e3-468f-b2b3-deb68119b320
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OES EYEPIECE HOOD
• Version Model Number: MB-326
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04953170063954 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K910423

FDA Product Code

• EOQ: BRONCHOSCOPE (FLEXIBLE OR RIGID)

Sterilization

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

[04953170063954]

Ethylene Oxide

[04953170063954]

Ethylene Oxide

[04953170063954]

Ethylene Oxide

[04953170063954]

Ethylene Oxide

[04953170063954]

Ethylene Oxide

[04953170063954]

Ethylene Oxide

[04953170063954]

Ethylene Oxide

[04953170063954]

Ethylene Oxide

[04953170063954]

Ethylene Oxide

[04953170063954]

Ethylene Oxide

[04953170063954]

Ethylene Oxide

[04953170063954]

Ethylene Oxide

[04953170063954]

Ethylene Oxide

[04953170063954]

Ethylene Oxide

[04953170063954]

Ethylene Oxide

[04953170063954]

Ethylene Oxide

[04953170063954]

Ethylene Oxide

[04953170063954]

Ethylene Oxide

[04953170063954]

Ethylene Oxide

[04953170063954]

Ethylene Oxide

[04953170063954]

Ethylene Oxide

[04953170063954]

Ethylene Oxide

[04953170063954]

Ethylene Oxide

[04953170063954]

Ethylene Oxide

[04953170063954]

Ethylene Oxide

[04953170063954]

Ethylene Oxide

Device Entry Metadata

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

Devices Manufactured by OLYMPUS MEDICAL SYSTEMS CORP.

• 04953170465949 - WATER CONTAINER: 2024-12-03
• 04953170465956 - WATER CONTAINER: 2024-12-03
• 04953170465963 - ENDOSCOPIC CO2 REGULATION UNIT: 2024-12-03
• 04953170465970 - EVIS EXERA III XENON LIGHT SOURCE: 2024-12-03
• 04953170454141 - VISERA S VIDEO SYSTEM CENTER: 2024-11-22
• 04953170452475 - EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE: 2024-10-14
• 04953170464935 - THUNDERBEAT 5 mm, 45 cm, Pistol Grip: 2024-09-17
• 04953170464973 - THUNDERBEAT 5 mm, 35 cm, Inline Grip: 2024-09-17