LabChoice Mechanical Pipette, Single Channel, Adjustable Volume 200-1000 uL

GUDID 00840117329737

Dynarex Corporation

Mechanical pipette

• Primary Device ID: 00840117329737
• NIH Device Record Key: cff1501f-df8a-4bcc-a8fe-16bd3c9c09f1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LabChoice Mechanical Pipette, Single Channel, Adjustable Volume 200-1000 uL
• Version Model Number: 40120
• Company DUNS: 008124539
• Company Name: Dynarex Corporation
• Device Count: 1
• 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: false
• 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	00840117329737 [Primary]
GS1	00840117330931 [Package]; Package: Shipper [50 Units]; In Commercial Distribution

FDA Product Code

• JRC: Micro Pipette

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: 2025-06-09
• Device Publish Date: 2025-05-30

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