IFE IgE Antiserum

GUDID M52594100

HELENA LABORATORIES CORPORATION

Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent

• Primary Device ID: M52594100
• NIH Device Record Key: 4de8157a-dada-4c7d-917e-5433dccd13a6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IFE IgE Antiserum
• Version Model Number: 9410
• Company DUNS: 079396131
• Company Name: HELENA LABORATORIES CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: 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

Customer Support Contacts

• Phone: +1(800)231-5663
• Email: helena@helena.com
• Phone: +1(800)231-5663
• Email: helena@helena.com
• Phone: +1(800)231-5663
• Email: helena@helena.com
• Phone: +1(800)231-5663
• Email: helena@helena.com
• Phone: +1(800)231-5663
• Email: helena@helena.com
• Phone: +1(800)231-5663
• Email: helena@helena.com
• Phone: +1(800)231-5663
• Email: helena@helena.com
• Phone: +1(800)231-5663
• Email: helena@helena.com
• Phone: +1(800)231-5663
• Email: helena@helena.com
• Phone: +1(800)231-5663
• Email: helena@helena.com
• Phone: +1(800)231-5663
• Email: helena@helena.com
• Phone: +1(800)231-5663
• Email: helena@helena.com
• Phone: +1(800)231-5663
• Email: helena@helena.com
• Phone: +1(800)231-5663
• Email: helena@helena.com
• Phone: +1(800)231-5663
• Email: helena@helena.com
• Phone: +1(800)231-5663
• Email: helena@helena.com
• Phone: +1(800)231-5663
• Email: helena@helena.com
• Phone: +1(800)231-5663
• Email: helena@helena.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M52594100 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K872834

FDA Product Code

• CZJ: IGD, ANTIGEN, ANTISERUM, CONTROL

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: 2023-09-11
• Device Publish Date: 2016-09-07

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• M52510680010 - SPIFE Touch, CSA 2015 (120V): 2023-09-11
• M52510690000 - SPIFE Touch (230V): 2023-09-11
• M52510880010 - SPIFE 3000 w/ New Pump & Valve (110V): 2023-09-11
• M52510880020 - SPIFE 3000, "CE 2011" (120V): 2023-09-11
• M52510890010 - SPIFE 3000 w/ New Pump & Valve (220V): 2023-09-11
• M52510890020 - SPIFE 3000, "CE 2011" (230V): 2023-09-11