Torq

GUDID 00862105000343

MiniDrive2

MEDTOX DIAGNOSTICS, INC.

General-purpose tabletop centrifuge

• Primary Device ID: 00862105000343
• NIH Device Record Key: 5337b97c-781f-41c6-8fc0-e8875036f527
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Torq
• Version Model Number: ZEA-MD2-1
• 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: true
• Lot Batch: false
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00862105000343 [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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2022-04-21
• Device Publish Date: 2021-05-28

On-Brand Devices [Torq]

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