EDINTRAK 4032-O

GUDID 07613327362589

Cannula

Stryker Trauma SA

Endoscope sheath, reusable

• Primary Device ID: 07613327362589
• NIH Device Record Key: 880256f0-94ec-4d3d-9eaf-0f9ce401daff
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EDINTRAK
• Version Model Number: 4032-O
• Catalog Number: 4032-O
• Company DUNS: 481999654
• Company Name: Stryker Trauma SA
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327362589 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K940230

FDA Product Code

• HRX: ARTHROSCOPE

Sterilization

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

[07613327362589]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-03-11
• Device Publish Date: 2017-05-30

On-Brand Devices [EDINTRAK]

• 37613327364300: Hook Blade
• 07613327364255: Hook Blade
• 37613327364232: Hook Blade
• 07613327364200: Hook Blade
• 07613327363265: Metatarsal Spreader
• 07613327363180: System
• 07613327363159: Micro Elevator
• 07613327362855: Obturator
• 07613327362848: Probe
• 07613327362831: System
• 07613327362770: Micro Blade Handle
• 07613327362749: Cannula
• 07613327362725: Sterilization Tray
• 07613327362688: Obturator
• 07613327362602: Micro Hook Blade
• 07613327362589: Cannula
• 07613327362480: Angled Micro Hook Blade
• 37613327362214: Micro Tip Swabs