Ziehm Vision FD

GUDID EZIEZIEHMVISIONFD1651

Mobile C-arm

Ziehm Imaging GmbH

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• Primary Device ID: EZIEZIEHMVISIONFD1651
• NIH Device Record Key: 48f986ce-0866-4ac4-8e7e-d9c9737c9a29
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ziehm Vision FD
• Version Model Number: Vision FD
• Company DUNS: 322720541
• Company Name: Ziehm Imaging 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: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	EZIEZIEHMVISIONFD1651 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K193230

FDA Product Code

• OWB: Interventional Fluoroscopic X-Ray System

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2023-07-31
• Device Publish Date: 2020-03-12

On-Brand Devices [Ziehm Vision FD]

• EZIEZIEHMVISIONFD165: 302891; 302929
• EZIEZIEHMVISIONFD1651: Mobile C-arm