IFA: BIOCHIP Sequence Legionella pneumophila (IgAG

GUDID 04049016052876

EUROIMMUN Medizinische Labordiagnostika AG

Legionella pneumophila total antibody IVD, kit, fluorescent immunoassay
Primary Device ID04049016052876
NIH Device Record Key0d65faf1-af11-4450-b304-758cb8df248a
Commercial Distribution Discontinuation2018-09-11
Commercial Distribution StatusNot in Commercial Distribution
Brand NameIFA: BIOCHIP Sequence Legionella pneumophila (IgAG
Version Model NumberFI 2150-1001 P
Company DUNS322209263
Company NameEUROIMMUN Medizinische Labordiagnostika AG
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Operating and Storage Conditions

Storage Environment TemperatureBetween 2 Degrees Celsius and 8 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS104049016052876 [Primary]

FDA Product Code

LHLReagents, Antibody, Legionella, Direct & Indirect Fluorescent

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-09-14
Device Publish Date2016-09-24

On-Brand Devices [IFA: BIOCHIP Sequence Legionella pneumophila (IgAG]

04049016052906FI 2150-2002 P
04049016052890FI 2150-2001 P
04049016052876FI 2150-1001 P

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