LE SOOTHE PINK POLYCHLOR PF EXAM PINK MED 431020

GUDID D7664310202

Smarthealth, Inc.

Polychloroprene examination/treatment glove, non-powdered Polychloroprene examination/treatment glove, non-powdered Polychloroprene examination/treatment glove, non-powdered Polychloroprene examination/treatment glove, non-powdered Polychloroprene examination/treatment glove, non-powdered Polychloroprene examination/treatment glove, non-powdered Polychloroprene examination/treatment glove, non-powdered Polychloroprene examination/treatment glove, non-powdered Polychloroprene examination/treatment glove, non-powdered Polychloroprene examination/treatment glove, non-powdered Polychloroprene examination/treatment glove, non-powdered Polychloroprene examination/treatment glove, non-powdered Polychloroprene examination/treatment glove, non-powdered Polychloroprene examination/treatment glove, non-powdered Polychloroprene examination/treatment glove, non-powdered Polychloroprene examination/treatment glove, non-powdered Polychloroprene examination/treatment glove, non-powdered

• Primary Device ID: D7664310202
• NIH Device Record Key: 6ebc9ce8-e4f1-48a2-854b-cb1bfc4963b2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LE SOOTHE PINK POLYCHLOR PF EXAM PINK MED
• Version Model Number: 431020
• Catalog Number: 431020
• Company DUNS: 061081477
• Company Name: Smarthealth, Inc.
• Device Count: 100
• 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: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D7664310200 [Unit of Use]
HIBCC	D7664310201 [Primary]
HIBCC	D7664310202 [Package]; Contains: D7664310201; Package: case [12 Units]; In Commercial Distribution

FDA Product Code

• LZA: Polymer 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: 2022-12-06
• Device Publish Date: 2022-11-28

Devices Manufactured by Smarthealth, Inc.

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• 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
• D766408732 - QUALITOUCH LATEX PF EXAM NATURAL CF MD: 2023-07-26 GLV QUALITOUCH LATEX PF EXAM NATURAL CF MED*100