STERILANCE

GUDID 36945630113865

Sterilance Medical (Suzhou) Inc.

Manual blood lancing device, reusable

• Primary Device ID: 36945630113865
• NIH Device Record Key: 5a49d5cb-f597-4583-8797-9b71f04abd08
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: STERILANCE
• Version Model Number: 02-2201
• Company DUNS: 554434897
• Company Name: Sterilance Medical (Suzhou) Inc.
• Device Count: 1
• 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	06945630113864 [Primary]
GS1	36945630113865 [Package]; Contains: 06945630113864; Package: [100 Units]; In Commercial Distribution

FDA Product Code

• QRL: Multiple Use Blood Lancet For Single Patient Use Only

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-09-20
• Device Publish Date: 2022-09-12

On-Brand Devices [STERILANCE]

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