Sterilance Press2 Pressure Activated Safety Lancet

GUDID 06945630109133

Sterilance Press2 Pressure Activated Safety Lancet,26G 1.8mm,50Lancets/box

SteriLance Medical (Suzhou) Inc.

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• Primary Device ID: 06945630109133
• NIH Device Record Key: f17a3290-d005-480f-b088-12ca8e9dfc48
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sterilance Press2 Pressure Activated Safety Lancet
• Version Model Number: 05-062618
• Company DUNS: 421141183
• Company Name: SteriLance Medical (Suzhou) Inc.
• Device Count: 50
• 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: false
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06945630109133 [Unit of Use]
GS1	16945630109130 [Primary]

FDA Product Code

• FMK: Lancet, Blood

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: 2020-12-29
• Device Publish Date: 2020-12-21

On-Brand Devices [Sterilance Press2 Pressure Activated Safety Lancet]

• 06945630109157: Sterilance Press2 Pressure Activated Safety Lancet,28G 1.8mm,100Lancets
• 06945630109140: Sterilance Press2 Pressure Activated Safety Lancet,28G 1.8mm,50Lancets
• 06945630109133: Sterilance Press2 Pressure Activated Safety Lancet,26G 1.8mm,50Lancets/box