ACTIN-F-PET

GUDID 10190302013147

LIFE TECHNOLOGIES CORPORATION

Nucleic acid hybridization detection IVD, probe
Primary Device ID10190302013147
NIH Device Record Keycaffd1fa-1b6a-43f0-854d-7bff8cfd248c
Commercial Distribution Discontinuation2020-03-30
Commercial Distribution StatusNot in Commercial Distribution
Brand NameACTIN-F-PET
Version Model NumberA13934
Company DUNS080131636
Company NameLIFE TECHNOLOGIES CORPORATION
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS110190302013147 [Primary]

FDA Product Code

MVUReagents, specific, analyte

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2020-04-06
Device Publish Date2018-09-18

Devices Manufactured by LIFE TECHNOLOGIES CORPORATION

10190302010320 - Human CD138 R-PE Conjugate2023-11-30
10190302010337 - Human CD138 PE-Cy®5.5 Conjugate2023-11-30
10190302011730 - Human CD61 APC Conjugate2023-11-30
10190302000680 - 3500Dx Series Polymer Pouch Caps2023-11-20
10190302000116 - Histostain® Plus Broad Spectrum2023-10-18
10190302000123 - invitrogen2023-10-18
10190302000130 - invitrogen2023-10-18
10190302008242 - Histostain® Plus 3rd Gen IHC Detection Kit (1000 Slides)2023-10-18

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.