242387

GUDID 10886705028825

LIGHT GUIDE, OLYMPUS - ACMI 5.0MM X 3.0M

Medos International Sàrl

Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable 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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• 10705034025483 - EXPEDIUM: 2024-07-08 EXPEDIUM SPINE SYSTEM POLYAXIAL BOLT, STANDARD 10 x 30mm
• 10705034025490 - EXPEDIUM: 2024-07-08 EXPEDIUM SPINE SYSTEM POLYAXIAL BOLT, STANDARD 10 x 35mm