Sterilance SteriHeel Plus

GUDID 16945630111935

Sterilance Medical (Suzhou) Inc.

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• Primary Device ID: 16945630111935
• NIH Device Record Key: f9760bea-0ed3-4999-b491-1991082dd151
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sterilance SteriHeel Plus
• Version Model Number: 30-101428
• Company DUNS: 554434897
• Company Name: Sterilance Medical (Suzhou) Inc.
• Device Count: 50
• 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: false
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06945630111938 [Unit of Use]
GS1	16945630111935 [Primary]

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: 2022-03-18
• Device Publish Date: 2022-03-10

Devices Manufactured by Sterilance Medical (Suzhou) Inc.

• 06945630125522 - STERiLANCE SteriHeel Plus Heel Incision Safety Lancet: 2024-04-17
• 26945630125120 - Disposable Safety Lancet Press2: 2024-04-08
• 36945630121808 - neoheel: 2024-02-16
• 36945630121815 - neoheel: 2024-02-16
• 06945630121821 - neoheel: 2024-02-16
• 36945630124106 - neoheel: 2024-02-16
• 26945630122846 - Soft: 2024-02-08
• 26945630122853 - Soft: 2024-02-08