Huahong

GUDID 00810011730441

Tianjin Huahong Technology Co., Ltd.

Manual blood lancing device, reusable

• Primary Device ID: 00810011730441
• NIH Device Record Key: ad901e88-f54f-4cc7-bbba-011374e86b9b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Huahong
• Version Model Number: HH-XVI-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	00810011730441 [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: 2023-08-24
• Device Publish Date: 2023-08-16

On-Brand Devices [Huahong]

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