External Marker Cover B

GUDID 04953170077753

OLYMPUS MEDICAL SYSTEMS CORP.

Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system Gastrointestinal catheter/endoscope tracking system

• Primary Device ID: 04953170077753
• NIH Device Record Key: b1ae1c5d-7cba-49d4-8d5b-8db858a80690
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: External Marker Cover B
• Version Model Number: MAJ-998
• 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: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04953170077753 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K002749

FDA Product Code

• PGU: Spatial Imaging For Display Of Endoscope Position

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: 2021-12-24
• Device Publish Date: 2021-12-16

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