FINDER

GUDID 00819704020388

FINDER Pipette, 50µL (pack of 5 pipettes)

BAEBIES, INC.

Mechanical pipette

• Primary Device ID: 00819704020388
• NIH Device Record Key: ae446758-8c3c-4f5d-a678-0283a2652786
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FINDER
• Version Model Number: 100-000020
• Company DUNS: 079264306
• Company Name: BAEBIES, INC.
• 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: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• 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	00819704020388 [Primary]

FDA Product Code

• JQW: Station, Pipetting And Diluting, For Clinical Use

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: 2025-02-10
• Device Publish Date: 2025-01-31

On-Brand Devices [FINDER]

• 00819704020395: FINDER Pipette, 50µL
• 00819704020388: FINDER Pipette, 50µL (pack of 5 pipettes)
• 00819704020364: FINDER G6PD TEST (Unit of Use)
• 00819704020340: FINDER G6PD Test (Box of 16)
• 00819704020333: FINDER Instrument