standard

GUDID 20810011730384

Tianjin Huahong Technology Co., Ltd.

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• Primary Device ID: 20810011730384
• NIH Device Record Key: 3f543041-f12a-4a7d-aacd-f360b82901d1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: standard
• Version Model Number: XXIII, 30G
• Company DUNS: 421272490
• Company Name: Tianjin Huahong Technology 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: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810011730380 [Unit of Use]
GS1	10810011730387 [Primary]
GS1	20810011730384 [Package]; Contains: 10810011730387; Package: carton [5000 Units]; In Commercial Distribution

FDA Product Code

• FMK: Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-02-22
• Device Publish Date: 2023-02-14

Devices Manufactured by Tianjin Huahong Technology Co., Ltd.

• 10810011730493 - Huahong: 2024-01-24
• 10810011730509 - Medhome: 2024-01-24
• 10810011730516 - Medhome: 2024-01-24
• 50810011730477 - Seren Guard: 2023-11-15
• 16957138606400 - Lite Touch: 2023-10-16
• 00810011730441 - Huahong: 2023-08-24
• 50810011730453 - HMD: 2023-08-24
• 50810011730460 - HMD: 2023-08-24