Motion Hybrid Wire Guide

GUDID 00827002448469

HERAEUS MEDICAL COMPONENTS LLC

Gastro-urological guidewire, single-use

• Primary Device ID: 00827002448469
• NIH Device Record Key: aba2f7c7-be1c-432f-9dbe-2e68d095c92c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Motion Hybrid Wire Guide
• Version Model Number: MHW-035150
• Company DUNS: 868303074
• Company Name: HERAEUS MEDICAL COMPONENTS LLC
• 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	00827002448469 [Primary]

FDA Product Code

• EZB: Stylet For Catheter, Gastro-Urology

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: 2021-09-17
• Device Publish Date: 2021-09-09

On-Brand Devices [Motion Hybrid Wire Guide]

• 00827002448551: MHWA-035150
• 00827002448490: MHWA-038150
• 00827002448483: MHW-038150
• 00827002448469: MHW-035150