Micro-X

GUDID 00858293006922

Micro-X Disinfectant/Sterilant

REPROCESSING PRODUCTS CORPORATION

Organic peroxy acid device sterilant, single-use

• Primary Device ID: 00858293006922
• NIH Device Record Key: b2926159-093e-455f-8ea5-477f2374f41a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Micro-X
• Version Model Number: MX-3212
• Company DUNS: 796083392
• Company Name: REPROCESSING PRODUCTS CORPORATION
• 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: 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: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00858293006922 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K962959

FDA Product Code

• MED: Sterilant, Medical Devices

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: 2023-02-28
• Device Publish Date: 2023-02-20

On-Brand Devices [Micro-X]

• 10858293006332: Micro-X Dialyzer Reprocessing Concentrate
• 00858293006120: Micro-X Peracetic Acid Test Strips - Potency
• 00858293006113: Micro-X Residual Test Strips
• 00858293006922: Micro-X Disinfectant/Sterilant