Gt Anti-Human IgG (Fc Sp.) FITC Conjugate

GUDID 10190302008945

LIFE TECHNOLOGIES CORPORATION

Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent

• Primary Device ID: 10190302008945
• NIH Device Record Key: 9a5e2677-b8ba-4851-a579-e1d2b482122b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Gt Anti-Human IgG (Fc Sp.) FITC Conjugate
• Version Model Number: H10001C
• Company DUNS: 080131636
• Company Name: LIFE TECHNOLOGIES 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: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10190302008945 [Primary]

FDA Product Code

• MVU: REAGENTS,SPECIFIC,ANALYTE

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-02-18
• Device Publish Date: 2018-03-07

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