STERiLANCE Soft Disposable Blood Lancet

GUDID 26945630132531

Sterilance Medical (Suzhou) Inc.

Blood lancet, single-use

• Primary Device ID: 26945630132531
• NIH Device Record Key: 1f23855a-348f-4a5b-a639-00b5b31c1fe6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: STERiLANCE Soft Disposable Blood Lancet
• Version Model Number: 01-0130
• Company DUNS: 554434897
• Company Name: Sterilance Medical (Suzhou) Inc.
• Device Count: 10
• 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: true
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06945630132537 [Unit of Use]
GS1	16945630132534 [Primary]
GS1	26945630132531 [Package]; Contains: 16945630132534; Package: [200 Units]; In Commercial Distribution
GS1	36945630132538 [Package]; Package: [5 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: 2024-10-31
• Device Publish Date: 2024-10-23

On-Brand Devices [STERiLANCE Soft Disposable Blood Lancet]

• 26945630117187: 01-0128
• 36945630117252: 01-0128
• 26945630132531: 01-0130