Sterilance

GUDID 36945630112769

Sterilance Medical (Suzhou) Inc.

Blood lancet, single-use

• Primary Device ID: 36945630112769
• NIH Device Record Key: b8e5eb67-72f7-4f36-91d0-1269db38011a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sterilance
• Version Model Number: 01-0121
• Company DUNS: 554434897
• Company Name: Sterilance Medical (Suzhou) Inc.
• Device Count: 100
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06945630112768 [Unit of Use]
GS1	16945630112765 [Primary]
GS1	36945630112769 [Package]; Contains: 16945630112765; Package: [50 Units]; In Commercial Distribution

FDA Product Code

• FMK: Single Use Only Blood Lancet With 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: 2022-07-08
• Device Publish Date: 2022-06-30

On-Brand Devices [Sterilance]

• 36945630112776: 01-0123
• 36945630112769: 01-0121
• 36945630113865: 02-2201