Torq

GUDID 00862105000374

Torq ZDrive MR, Ram Scientific

MEDTOX DIAGNOSTICS, INC.

General-purpose tabletop centrifuge

• Primary Device ID: 00862105000374
• NIH Device Record Key: 78dd0c23-9f59-4078-8f2a-af4e8b5cbc35
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Torq
• Version Model Number: ZZP-MR-RS Rev 0
• Company DUNS: 118569262
• Company Name: MEDTOX DIAGNOSTICS, INC.
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00862105000374 [Primary]

FDA Product Code

• JQC: Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-05-24
• Device Publish Date: 2022-05-16

On-Brand Devices [Torq]

• 00862105000343: MiniDrive2
• 00862105000374: Torq ZDrive MR, Ram Scientific