ReliOn

GUDID 00810011730212

Tianjin Huahong Technology Co., Ltd.

Manual blood lancing device, reusable

• Primary Device ID: 00810011730212
• NIH Device Record Key: 86dfc92c-36fc-4aa6-bd9e-f65bf794671a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ReliOn
• Version Model Number: HH-XIII-T
• Company DUNS: 421272490
• Company Name: Tianjin Huahong Technology Co., Ltd.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: true
• 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	00810011730212 [Primary]
GS1	10810011730219 [Package]; Package: case [500 Units]; In Commercial Distribution

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: 2022-06-07
• Device Publish Date: 2022-05-30

Devices Manufactured by Tianjin Huahong Technology Co., Ltd.

• 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
• 10810011730523 - GlucoDr.: 2025-04-24
• 50810011730583 - LinkSun: 2025-03-10
• 10810011730554 - BKG: 2024-11-01