Q-Wire System

GUDID 04250195604606

SOMATEX Medical Technologies GmbH

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• Primary Device ID: 04250195604606
• NIH Device Record Key: 55dc666d-ff97-4fc7-950a-4f56de57f55c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Q-Wire System
• Version Model Number: 271464
• Company DUNS: 341679629
• Company Name: SOMATEX Medical Technologies GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Unsafe
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250195603036 [Primary]
GS1	04250195604606 [Package]; Contains: 04250195603036; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• MIJ: Needle, Tumor Localization

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: 2021-11-05
• Device Publish Date: 2021-10-28

On-Brand Devices [Q-Wire System]

• 04250195604606: 271464
• 04250195604583: 271462
• 04250195604590: 271463