IFA: Legionella pneumophila Screening (Mix 1 / Mix

GUDID 04049016053309

EUROIMMUN Medizinische Labordiagnostika AG

Legionella pneumophila total antibody IVD, kit, fluorescent immunoassay

• Primary Device ID: 04049016053309
• NIH Device Record Key: a5804b76-ae85-4f17-b34c-6a415ad89f4a
• Commercial Distribution Discontinuation: 2018-09-11
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: IFA: Legionella pneumophila Screening (Mix 1 / Mix
• Version Model Number: FI 215b-1003-1 P
• 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	04049016053309 [Primary]

FDA Product Code

• LHL: Reagents, Antibody, Legionella, Direct & Indirect Fluorescent

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 [IFA: Legionella pneumophila Screening (Mix 1 / Mix]

• 04049016077848: FI 215b-2010-1 P
• 04049016053330: FI 215b-2005-1 P
• 04049016053323: FI 215b-1010-1 P
• 04049016053316: FI 215b-1005-1 P
• 04049016053309: FI 215b-1003-1 P