WIZDOM 512143

GUDID 20705032056318

SGW .014 WIZDOM SS 180 ST

CORDIS CORPORATION

Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use

• Primary Device ID: 20705032056318
• NIH Device Record Key: b538ab62-5586-4c4a-98c6-e5bf02515609
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: WIZDOM
• Version Model Number: 512143
• Catalog Number: 512143
• Company DUNS: 806136177
• Company Name: CORDIS 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: 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	10705032056311 [Primary]
GS1	20705032056318 [Package]; Contains: 10705032056311; Package: Box [5 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K953760

FDA Product Code

• DQX: Wire, guide, catheter

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: 2024-02-15
• Device Publish Date: 2024-02-07

On-Brand Devices [WIZDOM]

• 20705032056486: SGW .014 WIZ ST FLOPPY 300 ST
• 20705032056479: SGW .014 WIZ ST FLOPPY 180 J
• 20705032056462: SGW .014 WIZ ST FLOPPY 180 ST
• 20705032056349: SGW .014 WIZDOM SS 300 J
• 20705032056332: SGW .014 WIZDOM SS 300 ST
• 20705032056325: SGW .014 WIZDOM SS 180 J
• 20705032056295: SGW .014 WIZDOM SOFT 300 ST
• 20705032056288: SGW .014 WIZDOM SOFT 180 J
• 20705032056271: SGW .014 WIZDOM SOFT 180 ST
• 20705032056493: SGW .014 WIZ ST FLOPPY 300 J
• 20705032056318: SGW .014 WIZDOM SS 180 ST
• 20705032056301: SGW .014 WIZDOM SOFT 300 J