PORTABLE MEMORY

GUDID 04953170304965

OLYMPUS MEDICAL SYSTEMS CORP.

Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media Digital storage media

• Primary Device ID: 04953170304965
• NIH Device Record Key: 4ae248cb-dc53-4809-a487-6028284eae23
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PORTABLE MEMORY
• Version Model Number: MAJ-1925
• Company DUNS: 711789789
• Company Name: OLYMPUS MEDICAL SYSTEMS CORP.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)401-1086
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Device Identifiers

Device Issuing Agency	Device ID
GS1	04953170304965 [Primary]

FDA Product Code

• FEB: Accessories, Cleaning, For Endoscope
• LMB: Device, Digital Image Storage, Radiological

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-12-27
• Device Publish Date: 2021-12-18

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• 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