0233-050-064

GUDID 07613327051520

Fiberoptic Light Cable (Storz Scope and Stryker Light Source Fittings, Screw-On)

STRYKER CORPORATION

Fibreoptic light cable

• Primary Device ID: 07613327051520
• NIH Device Record Key: ec1b875d-a169-43a5-8b24-064cac262da9
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 0233050064
• Catalog Number: 0233-050-064
• Company DUNS: 187502109
• Company Name: STRYKER CORPORATION
• 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(866)624-4422
• Email: xx@xx.xx

Device Dimensions

• Length: 10 Feet
• Lumen/Inner Diameter: 5 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327051520 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K082813

FDA Product Code

• FCW: Light source, fiberoptic, routine

Sterilization

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

[07613327051520]

Hydrogen Peroxide;Moist Heat or Steam Sterilization;Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-23

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