Huahong

GUDID 10810011730639

Tianjin Huahong Technology Co., Ltd.

Manual blood lancing device, single-use

• Primary Device ID: 10810011730639
• NIH Device Record Key: 706ddd18-7873-4b7b-ad1a-6920ebd24fcc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Huahong
• Version Model Number: XXIII, 16G
• 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	00810011730632 [Primary]
GS1	10810011730639 [Package]; Contains: 00810011730632; Package: Case [50 Units]; In Commercial Distribution
GS1	50810011730637 [Unit of Use]

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: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-07-31
• Device Publish Date: 2025-07-23

On-Brand Devices [Huahong]

• 20810011730223: IK,28G
• 00810011730441: HH-XVI-T
• 10810011730493: I,30G
• 10810011730639: XXIII, 16G