suttersync

GUDID 36945630136673

Sterilance Medical (Suzhou) Inc.

Blood lancet, single-use

• Primary Device ID: 36945630136673
• NIH Device Record Key: f545370a-1d17-4e16-9f98-09ecdc9970fe
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: suttersync
• Version Model Number: soft 30G
• 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: 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	06945630136672 [Unit of Use]
GS1	16945630136679 [Primary]
GS1	36945630136673 [Package]; Contains: 16945630136679; Package: [200 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: 2025-06-02
• Device Publish Date: 2025-05-23

Devices Manufactured by Sterilance Medical (Suzhou) Inc.

• 26945630136669 - sutter sync: 2025-06-02
• 36945630136673 - suttersync: 2025-06-02
• 36945630136673 - suttersync: 2025-06-02
• 36945630136178 - TRANSTEK: 2025-04-30
• 36945630136147 - TRANSTEK: 2025-04-30
• 36945630136154 - TRANSTEK: 2025-04-30
• 26945630136164 - TRANSTEK: 2025-04-30
• 36945630135805 - Bard: 2025-03-31
• 06945630135316 - STERiLANCE OneStep Lancing Device: 2025-03-20