Packing

GUDID 04953170064753

MA-277 SPARE PACKING SPLINTING TUBE 12PK

OLYMPUS MEDICAL SYSTEMS CORP.

Intestinal splint

• Primary Device ID: 04953170064753
• NIH Device Record Key: 590f070b-467f-46ac-9fb0-e9f0e661ed6c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Packing
• Version Model Number: MA-277
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04953170064753 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K954451

FDA Product Code

• FET: Endoscopic video imaging system/component, gastroenterology-urology

Sterilization

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

[04953170064753]

High-level Disinfectant;Ethylene Oxide

[04953170064753]

High-level Disinfectant;Ethylene Oxide

[04953170064753]

High-level Disinfectant;Ethylene Oxide

[04953170064753]

High-level Disinfectant;Ethylene Oxide

[04953170064753]

High-level Disinfectant;Ethylene Oxide

[04953170064753]

High-level Disinfectant;Ethylene Oxide

[04953170064753]

High-level Disinfectant;Ethylene Oxide

[04953170064753]

High-level Disinfectant;Ethylene Oxide

[04953170064753]

High-level Disinfectant;Ethylene Oxide

[04953170064753]

High-level Disinfectant;Ethylene Oxide

[04953170064753]

High-level Disinfectant;Ethylene Oxide

[04953170064753]

High-level Disinfectant;Ethylene Oxide

[04953170064753]

High-level Disinfectant;Ethylene Oxide

[04953170064753]

High-level Disinfectant;Ethylene Oxide

[04953170064753]

High-level Disinfectant;Ethylene Oxide

[04953170064753]

High-level Disinfectant;Ethylene Oxide

[04953170064753]

High-level Disinfectant;Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-10-08
• Device Publish Date: 2016-09-21

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• 14953170440004 - THUNDERBEAT II Shears with Ultrasonic Mode, 5mm, 25cm: 2025-12-12
• 14953170440011 - THUNDERBEAT II Shears with Ultrasonic Mode, 5mm, 35cm: 2025-12-12
• 14953170440028 - THUNDERBEAT II Shears with Ultrasonic Mode, 5mm, 45cm: 2025-12-12
• 04953170442353 - ULTRASONIC BIPOLAR GENERATOR: 2025-12-12 "This product is Version 2. A Version 1 product with the same name exists."
• 04953170442445 - Update Tool for USG-410: 2025-12-12