REPROCESSING DATA CAPTURE UNIT

GUDID 04953170336935

OLYMPUS MEDICAL SYSTEMS CORP.

Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder Endoscope washer/disinfector data recorder

• Primary Device ID: 04953170336935
• NIH Device Record Key: dbe3a787-08e7-4455-a908-59dea7527174
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: REPROCESSING DATA CAPTURE UNIT
• Version Model Number: MAJ-2022
• 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
• 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	04953170336935 [Primary]

FDA Product Code

• OUG: Medical Device Data System

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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• 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