Anti-Mycoplasma pneumoniae IFA (IgA)

GUDID 04049016055112

EUROIMMUN Medizinische Labordiagnostika AG

Mycoplasma pneumoniae immunoglobulin A (IgA) antibody IVD, kit, fluorescent immunoassay

• Primary Device ID: 04049016055112
• NIH Device Record Key: 96b3f17b-9053-48dd-805e-b4c469fafdc8
• Commercial Distribution Discontinuation: 2018-09-11
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Anti-Mycoplasma pneumoniae IFA (IgA)
• Version Model Number: FI 2202-1005 A
• Company DUNS: 322209263
• Company Name: EUROIMMUN Medizinische Labordiagnostika AG
• 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: true
• 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

Operating and Storage Conditions

• Storage Environment Temperature: Between 2 Degrees Celsius and 8 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	04049016055112 [Primary]

FDA Product Code

• GRZ: Antisera, Fluorescent, All, Mycoplasma Spp.

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-09-14
• Device Publish Date: 2016-09-24

On-Brand Devices [Anti-Mycoplasma pneumoniae IFA (IgA)]

• 04049016078449: FI 2202-2010 A
• 04049016055136: FI 2202-2005 A
• 04049016055129: FI 2202-1010 A
• 04049016055112: FI 2202-1005 A
• 04049016055105: FI 2202-1003 A