HMD

GUDID 50810011730453

Tianjin Huahong Technology Co., Ltd.

Blood lancing device tip

• Primary Device ID: 50810011730453
• NIH Device Record Key: 1d34a8b2-bfc4-4044-a355-040a2d89d763
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HMD
• Version Model Number: IA,30G
• Company DUNS: 421272490
• Company Name: Tianjin Huahong Technology Co., Ltd.
• Device Count: 25
• 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	00810011730458 [Primary]
GS1	50810011730453 [Unit of Use]

FDA Product Code

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

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: 2023-08-24
• Device Publish Date: 2023-08-16

On-Brand Devices [HMD]

• 50810011730460: IA,30G
• 50810011730453: IA,30G