PERCUFIX 602-3001

GUDID 03700586902664

Instrument Set

Stryker GmbH

General internal orthopaedic fixation system implantation kit

• Primary Device ID: 03700586902664
• NIH Device Record Key: 3eff8a7a-b1cb-4507-b84b-19a6e94f8c4d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PERCUFIX
• Version Model Number: 602-3001
• Catalog Number: 602-3001
• Company DUNS: 481999654
• Company Name: Stryker GmbH
• 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	03700586902664 [Primary]

FDA Product Code

• JDW: PIN, FIXATION, THREADED

Sterilization

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

[03700586902664]

Moist Heat or Steam Sterilization

[03700586902664]

Moist Heat or Steam Sterilization

[03700586902664]

Moist Heat or Steam Sterilization

[03700586902664]

Moist Heat or Steam Sterilization

[03700586902664]

Moist Heat or Steam Sterilization

[03700586902664]

Moist Heat or Steam Sterilization

[03700586902664]

Moist Heat or Steam Sterilization

[03700586902664]

Moist Heat or Steam Sterilization

[03700586902664]

Moist Heat or Steam Sterilization

[03700586902664]

Moist Heat or Steam Sterilization

[03700586902664]

Moist Heat or Steam Sterilization

[03700586902664]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2025-04-14
• Device Publish Date: 2016-09-24

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