Control Set for the BD ProbeTec™ CT/GC/TV Qx Amplified DNA Assays 441925

GUDID 00382904419257

Control Set for the BD ProbeTec™ Chlamydia trachomatis/Neisseria gonorrhoeae/Trichomonas vaginalis (CT/GC/TV) Qx Amplified DNA Assays, 48

BECTON, DICKINSON AND COMPANY

Chlamydia trachomatis nucleic acid IVD, control Chlamydia trachomatis nucleic acid IVD, control
Primary Device ID00382904419257
NIH Device Record Key9c61dd9b-1f23-4f95-8753-60ac55559a25
Commercial Distribution StatusIn Commercial Distribution
Brand NameControl Set for the BD ProbeTec™ CT/GC/TV Qx Amplified DNA Assays
Version Model Number441925
Catalog Number441925
Company DUNS122561087
Company NameBECTON, DICKINSON AND COMPANY
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
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 Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)638-8663
EmailTechnical_services@bd.com
Phone+1(800)638-8663
EmailTechnical_services@bd.com

Operating and Storage Conditions

Storage Environment TemperatureBetween 2 Degrees Celsius and 33 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 33 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS100382904419257 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OUYTrichomonas vaginalis nucleic acid amplification test system

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-07-07

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