Fontus CFL8H02

GUDID 00812589020979

Fontus NGS LH, 8-96, IVD

Caliper Life Sciences, Inc.

Pipetting system IVD

• Primary Device ID: 00812589020979
• NIH Device Record Key: 01bd2d4c-aefb-4d24-a474-a6564ae8f264
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fontus
• Version Model Number: CFL8H02
• Catalog Number: CFL8H02
• Company DUNS: 933210197
• Company Name: Caliper Life Sciences, 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: false
• Lot Batch: false
• Serial Number: false
• 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	00812589020979 [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: 2024-07-10
• Device Publish Date: 2024-07-02

On-Brand Devices [Fontus]

• 00812589021136: Fontus LH, Standard, 8, IVD
• 00812589021129: Fontus LH, Expanded, 8, IVD
• 00812589021099: Fontus LH, Expanded, 8-384, IVD
• 00812589021082: Fontus LH, Standard, 8-384, IVD
• 00812589021075: Fontus LH, Expanded, 8-96, IVD
• 00812589021068: Fontus LH, Standard, 8-96, IVD
• 00812589021051: Fontus NGS LH, 8-384, IVD
• 00812589020979: Fontus NGS LH, 8-96, IVD