Advocate

GUDID 10810011730615

Tianjin Huahong Technology Co., Ltd.

Manual blood lancing device, single-use

• Primary Device ID: 10810011730615
• NIH Device Record Key: c9e1a35d-ac50-4202-b263-12966df6769e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Advocate
• Version Model Number: XVII, 21G
• 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	00810011730618 [Primary]
GS1	10810011730615 [Package]; Contains: 00810011730618; Package: Middle box [10 Units]; In Commercial Distribution
GS1	20810011730612 [Package]; Package: case [4 Units]; In Commercial Distribution
GS1	50810011730613 [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: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-06-27
• Device Publish Date: 2025-06-19

Devices Manufactured by Tianjin Huahong Technology Co., Ltd.

• 00810011730601 - Sinocare: 2025-06-27
• 10810011730615 - Advocate: 2025-06-27
• 10810011730615 - Advocate: 2025-06-27
• 30810011730336 - Care Touch: 2025-05-01
• 50810011730590 - LinkSun: 2025-05-01
• 10810011730523 - GlucoDr.: 2025-04-24
• 50810011730583 - LinkSun: 2025-03-10
• 10810011730554 - BKG: 2024-11-01
• 50810011730569 - GLUCORACYIK: 2024-11-01