Ultraproof MKH3-2

GUDID D832MKH322

Earloop Mask, Blue

PLASDENT CORPORATION

Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial Surgical/medical respirator, antimicrobial

• Primary Device ID: D832MKH322
• NIH Device Record Key: 358dc015-a7fe-40b0-ab8f-2ac759036a2e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ultraproof
• Version Model Number: MKH3-2
• Catalog Number: MKH3-2
• Company DUNS: 190377184
• Company Name: PLASDENT CORPORATION
• Device Count: 40
• 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: 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	D832MKH320 [Unit of Use]
HIBCC	D832MKH321 [Primary]
HIBCC	D832MKH322 [Package]; Contains: D832MKH321; Package: Case [20 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K133070

FDA Product Code

• FXX: Mask, Surgical

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: 2022-03-07
• Device Publish Date: 2022-02-25

On-Brand Devices [Ultraproof]

• D832MKH322: Earloop Mask, Blue
• D832MK362: Earloop Mask, Pink
• D832MK342: Earloop Mask, Green
• D832MK310L2: Earloop Mask, Lavender