STERILANCE Soft Disposable Blood Lancet

GUDID 26945630117187

Sterilance Medical (Suzhou) Inc.

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• Primary Device ID: 26945630117187
• NIH Device Record Key: 41793d3d-3cf2-4cf8-8182-cbf59a434efc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: STERILANCE Soft Disposable Blood Lancet
• Version Model Number: 01-0128
• Company DUNS: 554434897
• Company Name: Sterilance Medical (Suzhou) Inc.
• Device Count: 15
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06945630117183 [Unit of Use]
GS1	16945630117180 [Primary]
GS1	26945630117187 [Package]; Contains: 16945630117180; Package: [100 Units]; In Commercial Distribution
GS1	36945630117184 [Package]; Package: [6 Units]; In Commercial Distribution

FDA Product Code

• QRK: Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature

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: 2023-03-14
• Device Publish Date: 2023-03-06

On-Brand Devices [STERILANCE Soft Disposable Blood Lancet]

• 26945630117187: 01-0128
• 36945630117252: 01-0128