Anchorwire

GUDID 00816349011436

Lake Region Medical

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

• Primary Device ID: 00816349011436
• NIH Device Record Key: 5e97caea-fcfa-4b13-97b5-ea7718753639
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Anchorwire
• Version Model Number: LR1BG054
• Company DUNS: 031108704
• Company Name: Lake Region Medical
• 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: true
• 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 Dimensions

• Length: 230 Centimeter
• Length: 230 Centimeter
• Length: 230 Centimeter
• Length: 230 Centimeter
• Length: 230 Centimeter
• Length: 230 Centimeter

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *This guidewire should be store in a dry environment away from sunlight.

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816349011436 [Primary]

FDA Product Code

• GCA: Catheter, Biliary, Surgical

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-01-25

On-Brand Devices [Anchorwire]

• 00816349011436: LR1BG054
• 00816349010293: LR1BG043