Cytoclear Cytoplasm Remover GGS - JL004

GUDID 05060174130113

Cytoclear Cytoplasm Remover is a formulation which quickly dissolves and removes persistent cytoplasm during the methanol:acetic acid fixation stage of chromosome harvesting. In particular it dissolves the lipid and glycoprotein structure of which the cytoplasm is mainly composed

GENIAL HELIX LTD

Assay development analyte-specific reagent IVD Assay development analyte-specific reagent IVD Assay development analyte-specific reagent IVD Assay development analyte-specific reagent IVD Assay development analyte-specific reagent IVD Assay development analyte-specific reagent IVD Assay development analyte-specific reagent IVD Assay development analyte-specific reagent IVD Assay development analyte-specific reagent IVD Assay development analyte-specific reagent IVD Assay development analyte-specific reagent IVD Assay development analyte-specific reagent IVD Assay development analyte-specific reagent IVD Assay development analyte-specific reagent IVD Assay development analyte-specific reagent IVD Assay development analyte-specific reagent IVD Assay development analyte-specific reagent IVD

• Primary Device ID: 05060174130113
• NIH Device Record Key: 7b1241e2-5eaf-43c4-bf00-18776e018716
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cytoclear Cytoplasm Remover
• Version Model Number: GGS - JL004
• Catalog Number: GGS - JL004
• Company DUNS: 219918136
• Company Name: GENIAL HELIX LTD
• 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	05060174130113 [Primary]

FDA Product Code

• KIQ: Kit, Culture, Chromosome

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: 2023-09-26
• Device Publish Date: 2023-09-18

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