RETAINING RACK N4473701

GUDID 04953170437847

OLYMPUS MEDICAL SYSTEMS CORP.

Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack Sterilizer/disinfector rack

• Primary Device ID: 04953170437847
• NIH Device Record Key: a0374e6a-882d-4b84-b76f-f6a0705d472e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RETAINING RACK
• Version Model Number: MAJ-1970
• Catalog Number: N4473701
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04953170437847 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K103264

FDA Product Code

• FEB: Accessories, Cleaning, For Endoscope

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: 2023-04-28
• Device Publish Date: 2023-04-20

On-Brand Devices [RETAINING RACK]

• 04953170329616: MAJ-1970
• 04953170069611: MAJ-840
• 04953170437847: MAJ-1970
• 04953170438318: MAJ-840