CYLINDER PLUG

GUDID 04953170294877

MAJ-1940 FLEXCYSTO SUCTION PLUG CYF "A"

OLYMPUS MEDICAL SYSTEMS CORP.

Flexible video cystonephroscope Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable Endoscopic suction valve, reusable

• Primary Device ID: 04953170294877
• NIH Device Record Key: eea69a15-2b62-4396-b340-9be3dbd816ea
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CYLINDER PLUG
• Version Model Number: MAJ-1940
• 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
• 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	04953170294877 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K062049

FDA Product Code

• NWB: Endoscope, accessories, narrow band spectrum

Sterilization

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

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

[04953170294877]

Ethylene Oxide;Moist Heat or Steam Sterilization;High-level Disinfectant

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.

• 04953170452932 - TRACHEAL INTUBATION FIBERSCOPE: 2024-04-22
• 14953170460064 - Single Use Biliary Drainage Stent V: 2024-04-02
• 14953170460088 - Single Use Biliary Drainage Stent V: 2024-04-02
• 14953170460101 - Single Use Biliary Drainage Stent V: 2024-04-02
• 14953170460132 - Single Use Biliary Drainage Stent V: 2024-04-02
• 14953170460330 - Single Use Biliary Drainage Stent V: 2024-04-02
• 14953170460378 - Single Use Biliary Drainage Stent V: 2024-04-02
• 14953170460613 - Single Use Biliary Drainage Stent V: 2024-04-02