LabChoice Glass Test Tubes, 16 x 100 mm

GUDID 00810180841252

Dynarex Corporation

General laboratory container, single-use

• Primary Device ID: 00810180841252
• NIH Device Record Key: 1a8a4a68-6724-4a7f-9b1a-4776c7412cb0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LabChoice Glass Test Tubes, 16 x 100 mm
• Version Model Number: 42203
• Company DUNS: 008124539
• Company Name: Dynarex Corporation
• Device Count: 250
• 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: false
• 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	00810180841252 [Unit of Use]
GS1	00840117334977 [Package]; Contains: 00840117337534; Package: Case [4 Units]; In Commercial Distribution
GS1	00840117337534 [Primary]

FDA Product Code

• KJG: Tube, Tissue Culture

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: 2025-03-13
• Device Publish Date: 2025-03-05

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