Pro Comfort

GUDID 10810011730530

Tianjin Huahong Technology Co., Ltd.

Blood lancing device tip

• Primary Device ID: 10810011730530
• NIH Device Record Key: 4987c764-de63-4cf0-9849-87afa4ae6875
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pro Comfort
• Version Model Number: IK,30G
• Company DUNS: 421272490
• Company Name: Tianjin Huahong Technology Co., Ltd.
• Device Count: 310
• 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	00810011730533 [Primary]
GS1	10810011730530 [Package]; Contains: 00810011730533; Package: case [18600 Units]; In Commercial Distribution
GS1	50810011730538 [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: 2024-09-03
• Device Publish Date: 2024-08-26

On-Brand Devices [Pro Comfort]

• 10810011730547: IK,30G
• 10810011730530: IK,30G