DISPOSABLE BENDING CANNULA

GUDID 14953170044240

DISPOSABLE BENDING CANNULA

OLYMPUS MEDICAL SYSTEMS CORP.

Cholangiopancreatography catheter, single-use ERCP catheter, non-balloon, non-electrical, single-use ERCP catheter, non-balloon, non-electrical, single-use ERCP catheter, non-balloon, non-electrical, single-use ERCP catheter, non-balloon, non-electrical, single-use ERCP catheter, non-balloon, non-electrical, single-use ERCP catheter, non-balloon, non-electrical, single-use ERCP catheter, non-balloon, non-electrical, single-use ERCP catheter, non-balloon, non-electrical, single-use ERCP catheter, non-balloon, non-electrical, single-use ERCP catheter, non-balloon, non-electrical, single-use ERCP catheter, non-balloon, non-electrical, single-use ERCP catheter, non-balloon, non-electrical, single-use ERCP catheter, non-balloon, non-electrical, single-use ERCP catheter, non-balloon, non-electrical, single-use ERCP catheter, non-balloon, non-electrical, single-use ERCP catheter, non-balloon, non-electrical, single-use ERCP catheter, non-balloon, non-electrical, single-use ERCP catheter, non-balloon, non-electrical, single-use

• Primary Device ID: 14953170044240
• NIH Device Record Key: fd2bb18c-62d6-43bd-95b9-a42c4bfeb8d2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DISPOSABLE BENDING CANNULA
• Version Model Number: PR-233Q
• 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: false
• Labeled No Natural Rubber Latex: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04953170044243 [Primary]
GS1	14953170044240 [Package]; Contains: 04953170044243; Package: [1 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K011149

FDA Product Code

• ODD: Endoscopic retrograde cholangiopancreatography (ERCP) cannula

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

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• 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