ULTRATRACK Hybrid Guidewire 0.038" (0.97mm) x 150cm Regular Body, 3cm

GUDID 00821925031203

Gyrus Acmi, Inc.

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• Primary Device ID: 00821925031203
• NIH Device Record Key: 1968cac1-7087-4aa3-b3bb-70b70b6e2926
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ULTRATRACK Hybrid Guidewire 0.038" (0.97mm) x 150cm Regular Body, 3cm
• Version Model Number: GWH3805R
• Company DUNS: 007198742
• Company Name: Gyrus Acmi, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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	00821925031203 [Package]; Contains: 00821925031449; Package: [5 Units]; In Commercial Distribution
GS1	00821925031449 [Primary]

FDA Product Code

• EYA: STYLET, URETERAL

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-10-15
• Device Publish Date: 2018-09-13

On-Brand Devices [ULTRATRACK Hybrid Guidewire 0.038" (0.97mm) x 150cm Regular Body, 3cm]

• 00821925031210: GWH3805RA
• 00821925031203: GWH3805R