KINGFA

GUDID 06973163400021

Guangdong KINGFA SCI.&TECH. Co., Ltd.

Surgical/medical face mask, single-use

• Primary Device ID: 06973163400021
• NIH Device Record Key: d924a137-aba4-4e20-8a6a-49f422417719
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KINGFA
• Version Model Number: 1
• Company DUNS: 543265548
• Company Name: Guangdong KINGFA SCI.&TECH. 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: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06973163400021 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K201622

FDA Product Code

• FXX: Mask, Surgical

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: 2020-12-16
• Device Publish Date: 2020-12-08

On-Brand Devices [KINGFA]

• 06973163400021: 1
• 06973163400007: 1
• 16973163400066: KF-B P05
• 16973163400011: KF-B P05(L3)
• 26973163400100: KF-A F02(N)
• 26975390735017: nitrile examination gloves small size
• 26975390734973: nitrile examination gloves small size