242388

GUDID 10886705028832

LIGHT GUIDE, OLYMPUS - ACMI 5.0MM X 4.0M

Medos International Sàrl

Fibreoptic light cable

• Primary Device ID: 10886705028832
• NIH Device Record Key: 992f4a4e-cc44-42db-8df6-da4812235867
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 242388
• Catalog Number: 242388
• Company DUNS: 482661753
• Company Name: Medos International Sàrl
• 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: false
• 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)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10886705028832 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K901035

FDA Product Code

• FST: LIGHT, SURGICAL, FIBEROPTIC

Sterilization

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

[10886705028832]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028832]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028832]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028832]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028832]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028832]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028832]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028832]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028832]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028832]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028832]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028832]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028832]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028832]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028832]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028832]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2022-03-25
• Device Publish Date: 2017-10-26

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• 10886705022687 - RIGIDLOOP: 2026-03-31 RIGIDLOOP Cortical Fixation Implant 35mm
• 10886705022694 - RIGIDLOOP: 2026-03-31 RIGIDLOOP Cortical Fixation Implant 40mm
• 10886705022700 - RIGIDLOOP: 2026-03-31 RIGIDLOOP Cortical Fixation Implant 45mm
• 10886705022717 - RIGIDLOOP: 2026-03-31 RIGIDLOOP Cortical Fixation Implant 50mm