Pseudomonas-CF-IgG standard control serum 60900

GUDID 05713106609002

Human-antisera, Pseudomonas-CF-IgG

Ssi Diagnostica A/S

Pseudomonas aeruginosa immunoglobulin G (IgG) antibody IVD, control

• Primary Device ID: 05713106609002
• NIH Device Record Key: a98eb715-c4a9-4ddb-bc2c-b2854cc27f86
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pseudomonas-CF-IgG standard control serum
• Version Model Number: 60900
• Catalog Number: 60900
• Company DUNS: 305684449
• Company Name: Ssi Diagnostica A/S
• 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: false
• Manufacturing Date: false
• Expiration Date: true
• 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	05713106609002 [Primary]

FDA Product Code

• GSS: Antisera, Fluorescent, Pseudomonas Aeruginosa

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-16

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