DISPOSABLE BALLOON CATHETER

GUDID 14953170047463

OLYMPUS MEDICAL SYSTEMS CORP.

Bronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter Gastrointestinal/tracheobronchial balloon catheter

• Primary Device ID: 14953170047463
• NIH Device Record Key: d0029e9d-d6db-411b-8945-bdeaa9f60b6e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DISPOSABLE BALLOON CATHETER
• Version Model Number: B7-2C
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• 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
• 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	04953170047466 [Primary]
GS1	14953170047463 [Package]; Contains: 04953170047466; Package: [1 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K962901

FDA Product Code

• EOQ: BRONCHOSCOPE (FLEXIBLE OR RIGID)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-21

On-Brand Devices [DISPOSABLE BALLOON CATHETER]

• 14953170047487: DISPOSABLE BALLOON CATHETER
• 14953170047463: B7-2C
• 14953170047449: DISPOSABLE BALLOON CATHETER
• 14953170047395: DISPOSABLE BALLOON CATHETER
• 14953170047371: DISPOSABLE BALLOON CATHETER
• 14953170463751: B5-2Q
• 14953170463706: B7-2Q
• 14953170463683: B7-2LA