242387

GUDID 10886705028825

LIGHT GUIDE, OLYMPUS - ACMI 5.0MM X 3.0M

Medos International Sàrl

Fibreoptic light cable

• Primary Device ID: 10886705028825
• NIH Device Record Key: c4c5c5c3-427c-4102-8d47-b4d922fc5552
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 242387
• Catalog Number: 242387
• 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	10886705028825 [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

[10886705028825]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028825]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028825]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028825]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028825]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028825]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028825]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028825]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028825]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028825]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028825]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028825]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028825]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028825]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028825]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[10886705028825]

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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• 10705034596891 - TRIALTIS: 2024-08-26 TRIALTIS Spine System Set Screw 2 Pack T27 5.5 and 6.0
• 10705034596907 - TRIALTIS: 2024-08-26 TRIALTIS Spine System Set Screw 6 Pack T27 5.5 and 6.0
• 10705034199504 - VIPER: 2024-08-20 VIPER SYSTEM CANNULA PLUNGER
• 10705034062358 - MONARCH: 2024-07-29 MONARCH SPINE SYSTEM S/C WITH WASHER, STRAIGHT 5.5mm