LabChoice Transfer Pipettes, Small Bulb, 3mL

GUDID 00810180840774

Non-Sterile

Dynarex Corporation

Pipette tip IVD

• Primary Device ID: 00810180840774
• NIH Device Record Key: 80de1dd5-77d4-4828-b406-1d99782d9fde
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LabChoice Transfer Pipettes, Small Bulb, 3mL
• Version Model Number: 40202
• Company DUNS: 008124539
• Company Name: Dynarex Corporation
• Device Count: 500
• 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	00810180840774 [Unit of Use]
GS1	00840117329942 [Package]; Contains: 00840117336513; Package: Case [10 Units]; In Commercial Distribution
GS1	00840117336513 [Primary]

FDA Product Code

• GJW: Pipette, Pasteur

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: 2025-01-02
• Device Publish Date: 2024-12-25

Devices Manufactured by Dynarex Corporation

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• 00810180840774 - LabChoice Transfer Pipettes, Small Bulb, 3mL: 2025-01-02Non-Sterile
• 00810180840774 - LabChoice Transfer Pipettes, Small Bulb, 3mL: 2025-01-02 Non-Sterile
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• 00840117340411 - Resp-O2 Disposable Guedel Airway, 110 mm, Adult X-Large, Orange: 2024-12-30