Sterilance Soft Disposable Blood Lancet

GUDID 36945630117252

Sterilance Medical (Suzhou) Inc.

Blood lancet, single-use

• Primary Device ID: 36945630117252
• NIH Device Record Key: 9c7a3f2e-9289-42a0-8099-3836815ab908
• 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: 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: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06945630117251 [Unit of Use]
GS1	16945630117258 [Primary]
GS1	36945630117252 [Package]; Contains: 16945630117258; Package: [1000 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: 2023-03-21
• Device Publish Date: 2023-03-13

On-Brand Devices [Sterilance Soft Disposable Blood Lancet]

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