Health-Tec/DHP Pro-Tec Latex Exam Gloves 410-PPFXL2

GUDID D773410PPFXL21

Health-Tec/DHP Pro-Tec Latex Exam Gloves Non-Chlorinated Size X-Large

Dental Health Products Inc

Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial

• Primary Device ID: D773410PPFXL21
• NIH Device Record Key: 4e8a9c80-a645-450e-9ba3-5b332ce15737
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Health-Tec/DHP Pro-Tec Latex Exam Gloves
• Version Model Number: 410-PPFXL2
• Catalog Number: 410-PPFXL2
• Company DUNS: 623191194
• Company Name: Dental Health Products Inc
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D773410PPFXL21 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K000999

FDA Product Code

• LYY: Latex Patient Examination Glove

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: 2022-09-29
• Device Publish Date: 2022-09-21

On-Brand Devices [Health-Tec/DHP Pro-Tec Latex Exam Gloves]

• D773410PPFXS21: Health-Tec/DHP Pro-Tec Latex Exam Gloves Non-Chlorinated Size X-Small 100/box
• D773410PPFXL21: Health-Tec/DHP Pro-Tec Latex Exam Gloves Non-Chlorinated Size X-Large
• D773410PPFS21: Health-Tec/DHP Pro-Tec Latex Exam Gloves Non-Chlorinated Size Small 100/box
• D773410PPFM21: Health-Tec/DHP Pro-Tec Latex Exam Gloves Non-Chlorinated Size Medium 100/box
• D773410PPFL21: Health-Tec/DHP Pro-Tec Latex Exam Gloves Non-Chlorinated Size Large 100/box