Allevy

GUDID 00810011730663

Tianjin Huahong Technology Co., Ltd.

Manual blood lancing device, reusable

• Primary Device ID: 00810011730663
• NIH Device Record Key: 060d8c2c-a7bc-4bfe-a795-299f501eb612
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Allevy
• Version Model Number: HH-X-T
• Company DUNS: 421272490
• Company Name: Tianjin Huahong Technology 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810011730663 [Primary]

FDA Product Code

• QRL: Multiple Use Blood Lancet For Single Patient Use Only

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: 2026-01-01
• Device Publish Date: 2025-12-24

Devices Manufactured by Tianjin Huahong Technology Co., Ltd.

• 50810011730644 - Huahong: 2026-01-01
• 00810011730656 - Huahong: 2026-01-01
• 00810011730663 - Allevy: 2026-01-01
• 00810011730663 - Allevy: 2026-01-01
• 10810011730639 - Huahong: 2025-07-31
• 00810011730601 - Sinocare: 2025-06-27
• 10810011730615 - Advocate: 2025-06-27
• 30810011730336 - Care Touch: 2025-05-01
• 50810011730590 - LinkSun: 2025-05-01