KINGFA MEDICAL

GUDID 26973163403217

Medium size

Guangdong KINGFA SCI.&TECH. 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: 26973163403217
• NIH Device Record Key: 5f8a082c-9f8a-40f2-94a5-07fd5a2690fe
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KINGFA MEDICAL
• Version Model Number: KG-1601
• Company DUNS: 543265548
• Company Name: Guangdong KINGFA SCI.&TECH. Co., Ltd.
• 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: true
• 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
GS1	06973163403213 [Unit of Use]
GS1	16973163403210 [Primary]
GS1	26973163403217 [Package]; Contains: 16973163403210; Package: carton [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K203593

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: 2021-05-18
• Device Publish Date: 2021-05-10

On-Brand Devices [KINGFA MEDICAL]

• 26973163403231: Extra large size
• 26973163403224: Large size
• 26973163403217: Medium size
• 26973163403200: Small size
• 26973163403118: Extra large size
• 26973163403101: Large size
• 26973163403095: Medium size
• 26973163403088: Small size
• 26973163402968: Extra large size
• 26973163402951: Large size
• 26973163402944: Medium size
• 06973163402933: Small size
• 06973163404197: KF-A F02(N)
• 06973163406184: KF-B P05(L3)