Flexvision 0233032800

GUDID 07613327051490

Sterilization Tray for Flexible Urology Instruments

STRYKER CORPORATION

Sterilization container Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable

• Primary Device ID: 07613327051490
• NIH Device Record Key: 31c4bbed-4cc6-4369-ae32-11ecfa603b64
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Flexvision
• Version Model Number: 0233032800
• Catalog Number: 0233032800
• 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
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327051490 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K935237

FDA Product Code

• FGB: Ureteroscope and accessories, flexible/rigid

Sterilization

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

[07613327051490]

Moist Heat or Steam Sterilization

[07613327051490]

Moist Heat or Steam Sterilization

[07613327051490]

Moist Heat or Steam Sterilization

[07613327051490]

Moist Heat or Steam Sterilization

[07613327051490]

Moist Heat or Steam Sterilization

[07613327051490]

Moist Heat or Steam Sterilization

[07613327051490]

Moist Heat or Steam Sterilization

[07613327051490]

Moist Heat or Steam Sterilization

[07613327051490]

Moist Heat or Steam Sterilization

[07613327051490]

Moist Heat or Steam Sterilization

[07613327051490]

Moist Heat or Steam Sterilization

[07613327051490]

Moist Heat or Steam Sterilization

[07613327051490]

Moist Heat or Steam Sterilization

[07613327051490]

Moist Heat or Steam Sterilization

[07613327051490]

Moist Heat or Steam Sterilization

[07613327051490]

Moist Heat or Steam Sterilization

[07613327051490]

Moist Heat or Steam Sterilization

[07613327051490]

Moist Heat or Steam Sterilization

[07613327051490]

Moist Heat or Steam Sterilization

[07613327051490]

Moist Heat or Steam Sterilization

[07613327051490]

Moist Heat or Steam Sterilization

[07613327051490]

Moist Heat or Steam Sterilization

[07613327051490]

Moist Heat or Steam Sterilization

[07613327051490]

Moist Heat or Steam Sterilization

[07613327051490]

Moist Heat or Steam Sterilization

[07613327051490]

Moist Heat or Steam Sterilization

[07613327051490]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-23

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• 07613327627701 - KNOTILUS+: 2024-03-15 2.4X8.9MM KNOTILUS+ HIP ANCHOR - PEEK
• 07613327623796 - KNOTILUS+: 2024-03-13 2.4X8.9MM DRILL, HIP
• 07613327623833 - KNOTILUS+: 2024-03-13 2.4X8.9MM DRILL, HARD BONE, HIP
• 07613327634686 - Iconix: 2024-03-12 Iconix DC Guide for 1.4mm anchor
• 07613327634693 - Iconix: 2024-03-12
• 07613327616675 - SPY: 2024-03-06