Suhui

GUDID 06974466380140

Nitrile Examination Gloves, XL, Black

Zhenjiang Suhui Latex Products Co., Ltd

Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial

• Primary Device ID: 06974466380140
• NIH Device Record Key: 4de17ee3-3321-40af-bb3b-243d85f1b630
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Suhui
• Version Model Number: Nitrile
• Company DUNS: 530808336
• Company Name: Zhenjiang Suhui Latex Products Co., Ltd
• 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: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06974466380140 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K211778

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: 2021-10-28
• Device Publish Date: 2021-10-20

On-Brand Devices [Suhui]

• 06974466380140: Nitrile Examination Gloves, XL, Black
• 06974466380133: Nitrile Examination Gloves, XS, Black
• 06974466380126: Nitrile Examination Gloves, M, Black
• 06974466380119: Nitrile Examination Gloves, S, Black
• 06974466380102: Nitrile Examination Gloves, XS, Black
• 06974466380096: Nitrile Examination Gloves, XL, Blue
• 06974466380089: Nitrile Examination Gloves, L, Blue
• 06974466380072: Nitrile Examination Gloves, M, Blue
• 06974466380065: Nitrile Examination Gloves, S, Blue
• 06974466380041: Nitrile Examination Gloves, XL, GREEN
• 06974466380034: Nitrile Examination Gloves, L, GREEN
• 06974466380003: Nitrile Examination Gloves, XS, GREEN
• 06974466380058: Nitrile Examination Gloves, XS, Blue
• 06974466380027: Nitrile Examination Gloves, M, GREEN
• 06974466380010: Nitrile Examination Gloves, S, GREEN