0406-760-000

GUDID 07613154498611

Parallel Bipolar Adapter Cable

STRYKER CORPORATION

Radio-frequency ablation system generator

• Primary Device ID: 07613154498611
• NIH Device Record Key: 9813e953-950a-4db4-bdfa-48bc5597f530
• Commercial Distribution Discontinuation: 2018-12-31
• Commercial Distribution Status: Not in Commercial Distribution
• Version Model Number: 0406760000
• Catalog Number: 0406-760-000
• Company DUNS: 196548481
• 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(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613154498611 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K061660

FDA Product Code

• GEI: ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

Sterilization

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

[07613154498611]

Moist Heat or Steam Sterilization

[07613154498611]

Moist Heat or Steam Sterilization

[07613154498611]

Moist Heat or Steam Sterilization

[07613154498611]

Moist Heat or Steam Sterilization

[07613154498611]

Moist Heat or Steam Sterilization

[07613154498611]

Moist Heat or Steam Sterilization

[07613154498611]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-11-22
• Device Publish Date: 2016-09-23

Devices Manufactured by STRYKER CORPORATION

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• 07613327624083 - Echo: 2025-02-03 Intracranial Base Catheter
• 07613327624106 - Broadway 8: 2025-02-03 Catheter
• 37613327548205 - Neptune SafeAir: 2025-01-14 Telescopic Smoke Evacuation Pencil, Push Button, Coated, No PVC
• 07613327273120 - TRIO: 2025-01-03 PEDICULAR SCREWDRIVER SHAFT
• 07613327273144 - TRIO +: 2025-01-03 SELF HOLDING PEDICULAR SCREWDRIVER
• 07613327273175 - TRIO +: 2025-01-03 FLEXIBLE EXTENDER III