FDA.reportPublic FDA data

UDI TEST SKU

Primary DI
37503025060232
Brand
UDI TEST SKU
Company
LIFE TECHNOLOGIES CORPORATION
Model
A40401 TST
Device description
UDI TEST SKU Device Description
Published
2018-06-02
Public version status
New
Distribution status
Not in Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Product Codes#

Code, Name table
CodeName
FMHCONTAINER, SPECIMEN, STERILE

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FMHContainer, Specimen, SterilePathology1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
37503025060232PackageGS1100Not in Commercial Distribution
17503025060238PrimaryGS10
87503025060237Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized table
Source identifierGTIN-14 normalized
3750302506023237503025060232
1750302506023817503025060238
8750302506023787503025060237

GMDN Terms#

Term, Definition table
TermDefinition
General-purpose tabletop centrifugeA tabletop- or bench-mounted mains electricity (AC-powered) device used mainly in the clinical laboratory to separate the components of suspensions through low- or medium-speed centrifugal force (typically up to 6,000 or 12,000 rpm). It is typically a compact stationary structure with an electric motor, a vertical shaft, and a horizontal rotor attached to the upper end. This device is mostly used to centrifuge various patient samples (i.e., body fluids), either alone or after addition of reagents or other additives before measuring analytes.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
118793157
Device count
5
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
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10190302018999TaqPath™ COVID-19, Flu A, Flu B, RSV Select Positive Control9636122025-02-17
10190302019002TaqPath™ COVID-19, Flu A, Flu B, RSV Select Negative Control9636092025-02-17
10190302019019TaqPath™ 1-Step Select Master Mix (No ROX)A56518A561232025-02-17
10190302019026TaqPath™ COVID-19, Flu A, Flu B, RSV Select AssayA564412025-02-17
10190302019033TaqPath™ COVID-19, Flu A, Flu B, RSV Select Positive Control9636132025-02-17
10190302019040TaqPath™ COVID-19, Flu A, Flu B, RSV Select Negative Control9636082025-02-17
10190302019057TaqPath™ 1-Step Select Master Mix (No ROX)A565192025-02-17
10190302019422Applied Biosystems™ TaqPath™ COVID-19 Diagnostic PCR Assay KitA572972025-02-17
80190302019438Applied Biosystems™ TaqPath™ COVID-19 Diagnostic PCR Control Dilution BufferA577402025-02-17
10190302019446Applied Biosystems™ TaqPath™ COVID-19 Diagnostic PCR Control9661362025-02-17
10190302006385Oncomine™ Dx Target TestA324412017-06-27
10190302005197Aim -V™ MediumA18398DJ2016-08-01
10190302012041Human CD99 FITC ConjugateMHCD99012018-06-15
10190302012058Human CD99 R-PE ConjugateMHCD99042018-06-15
10190302012065Human CXCR4 (CD184) R-PE ConjugateMHCXCR4042018-06-15
10190302012164Anti-Human HLA-DR (Class II) FITC ConjugateMHLDR012018-06-15
10190302012171Anti-Human HLA-DR (Class II) R-PE ConjugateMHLDR042018-06-15
10190302012188Anti-Human HLA-DR (Class II) APC ConjugateMHLDR052018-06-15
10190302012195Anti-Human HLA-DR (Class II) PE-Texas Red® ConjugateMHLDR172018-06-15

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Primary DI, Brand, Company table
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H108117393CorningCorning IncorporatedFMH2026-01-14
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30815112021482TranspecBracco Diagnostics Inc.FMH2026-01-09
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