QUALITOUCH LATEX PF L/R FIT EXAM NATURAL 9 43190

GUDID D766431902

GLV QUALITOUCH LATEX PF L/R FIT NATURAL 9.0*45 PR

Smarthealth, Inc.

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

• Primary Device ID: D766431902
• NIH Device Record Key: b7be66a7-a39d-4ce6-a2b2-fa81e3abd576
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: QUALITOUCH LATEX PF L/R FIT EXAM NATURAL 9
• Version Model Number: 43190
• Catalog Number: 43190
• Company DUNS: 061081477
• Company Name: Smarthealth, Inc.
• Device Count: 45
• DM Exempt: true
• 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

Customer Support Contacts

• Phone: 1-800-522-0800
• Email: info@smartpractice.com
• Phone: 1-800-522-0800
• Email: info@smartpractice.com
• Phone: 1-800-522-0800
• Email: info@smartpractice.com
• Phone: 1-800-522-0800
• Email: info@smartpractice.com
• Phone: 1-800-522-0800
• Email: info@smartpractice.com
• Phone: 1-800-522-0800
• Email: info@smartpractice.com
• Phone: 1-800-522-0800
• Email: info@smartpractice.com
• Phone: 1-800-522-0800
• Email: info@smartpractice.com
• Phone: 1-800-522-0800
• Email: info@smartpractice.com
• Phone: 1-800-522-0800
• Email: info@smartpractice.com
• Phone: 1-800-522-0800
• Email: info@smartpractice.com
• Phone: 1-800-522-0800
• Email: info@smartpractice.com
• Phone: 1-800-522-0800
• Email: info@smartpractice.com
• Phone: 1-800-522-0800
• Email: info@smartpractice.com
• Phone: 1-800-522-0800
• Email: info@smartpractice.com
• Phone: 1-800-522-0800
• Email: info@smartpractice.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Operating and Storage Conditions

• Storage Environment Temperature: Between 0 Degrees Fahrenheit and 104 Degrees Fahrenheit
• Storage Environment Temperature: Between 0 Degrees Fahrenheit and 104 Degrees Fahrenheit
• Storage Environment Temperature: Between 0 Degrees Fahrenheit and 104 Degrees Fahrenheit
• Storage Environment Temperature: Between 0 Degrees Fahrenheit and 104 Degrees Fahrenheit
• Storage Environment Temperature: Between 0 Degrees Fahrenheit and 104 Degrees Fahrenheit
• Storage Environment Temperature: Between 0 Degrees Fahrenheit and 104 Degrees Fahrenheit
• Storage Environment Temperature: Between 0 Degrees Fahrenheit and 104 Degrees Fahrenheit
• Storage Environment Temperature: Between 0 Degrees Fahrenheit and 104 Degrees Fahrenheit
• Storage Environment Temperature: Between 0 Degrees Fahrenheit and 104 Degrees Fahrenheit
• Storage Environment Temperature: Between 0 Degrees Fahrenheit and 104 Degrees Fahrenheit
• Storage Environment Temperature: Between 0 Degrees Fahrenheit and 104 Degrees Fahrenheit
• Storage Environment Temperature: Between 0 Degrees Fahrenheit and 104 Degrees Fahrenheit
• Storage Environment Temperature: Between 0 Degrees Fahrenheit and 104 Degrees Fahrenheit
• Storage Environment Temperature: Between 0 Degrees Fahrenheit and 104 Degrees Fahrenheit
• Storage Environment Temperature: Between 0 Degrees Fahrenheit and 104 Degrees Fahrenheit
• Storage Environment Temperature: Between 0 Degrees Fahrenheit and 104 Degrees Fahrenheit

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D766431900 [Unit of Use]
HIBCC	D766431901 [Primary]
HIBCC	D766431902 [Package]; Contains: D766431901; Package: case [10 Units]; In Commercial Distribution

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: 2023-07-26
• Device Publish Date: 2023-07-18

Devices Manufactured by Smarthealth, Inc.

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• D7664311062 - REFLECTION SAPPHIRE SENSITIVE NITRILE PF EXAM XS: 2023-08-15 GLV REFLECTION SAPPHIRE SENSITIVE NITRILE PF EXAM XS*200
• D7664311072 - REFLECTION SAPPHIRE SENSITIVE NITRILE PF EXAM SM: 2023-08-15 GLV REFLECTION SAPPHIRE SENSITIVE NITRILE PF EXAM SM*200
• D7664311082 - REFLECTION SAPPHIRE SENSITIVE NITRILE PF EXAM MED: 2023-08-15 GLV REFLECTION SAPPHIRE SENSITIVE NITRILE PF EXAM MED*200
• D7664311092 - REFLECTION SAPPHIRE SENSITIVE NITRILE PF EXAM LG: 2023-08-15 GLV REFLECTION SAPPHIRE SENSITIVE NITRILE PF EXAM LG*200
• D7664311102 - REFLECTION SAPPHIRE SENSITIVE NITRILE PF EXAM XL: 2023-08-15 GLV REFLECTION SAPPHIRE SENSITIVE NITRILE PF EXAM XL*200
• D766408712 - QUALITOUCH LATEX PF EXAM NATURAL CF XS*: 2023-07-26 GLV QUALITOUCH LATEX PF EXAM NATURAL CF XS*100
• D766408722 - QUALITOUCH LATEX PF EXAM NATURAL CF SM: 2023-07-26 GLV QUALITOUCH LATEX PF EXAM NATURAL CF SM*100