TRANSTEK

GUDID 26945630136164

Sterilance Medical (Suzhou) Inc.

Manual blood lancing device, reusable

• Primary Device ID: 26945630136164
• NIH Device Record Key: 09abd0a8-4e04-4081-8928-1932278895ae
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TRANSTEK
• Version Model Number: "LDE4 02-2201"
• Company DUNS: 554434897
• Company Name: Sterilance Medical (Suzhou) Inc.
• Device Count: 1
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	16945630136167 [Primary]
GS1	26945630136164 [Package]; Contains: 16945630136167; Package: [50 Units]; In Commercial Distribution
GS1	36945630136161 [Package]; Package: [10 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: 2025-04-30
• Device Publish Date: 2025-04-22

On-Brand Devices [TRANSTEK]

• 26945630136164: "LDE4 02-2201"
• 36945630136154: Soft 30G 01-0130
• 36945630136147: Soft 30G 01-0130
• 36945630136178: "LDE4 02-2201"