HUAHONG

GUDID 20810011730223

Tianjin Huahong Technology Co., Ltd.

Blood lancet, single-use

• Primary Device ID: 20810011730223
• NIH Device Record Key: 83449918-eeb7-4900-aca6-4cf3210784ce
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HUAHONG
• Version Model Number: IK,28G
• Company DUNS: 421272490
• Company Name: Tianjin Huahong Technology Co., Ltd.
• Device Count: 10
• DM Exempt: false
• 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: 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	00810011730229 [Unit of Use]
GS1	10810011730226 [Primary]
GS1	20810011730223 [Package]; Contains: 10810011730226; Package: Carton [20000 Units]; In Commercial Distribution

FDA Product Code

• QRK: Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature
• 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: 2022-06-07
• Device Publish Date: 2022-05-30

On-Brand Devices [HUAHONG]

• 20810011730223: IK,28G
• 00810011730441: HH-XVI-T
• 10810011730493: I,30G
• 10810011730639: XXIII, 16G