642VFD Plus Centrifuge, Selphyl US/CAN 00-027-055-001

GUDID 00810052861555

General purpose laboratory centrifuge for sample separation.

DRUCKER DIAGNOSTICS

General-purpose tabletop centrifuge General-purpose tabletop centrifuge General-purpose tabletop centrifuge General-purpose tabletop centrifuge General-purpose tabletop centrifuge General-purpose tabletop centrifuge General-purpose tabletop centrifuge General-purpose tabletop centrifuge General-purpose tabletop centrifuge General-purpose tabletop centrifuge General-purpose tabletop centrifuge General-purpose tabletop centrifuge General-purpose tabletop centrifuge General-purpose tabletop centrifuge General-purpose tabletop centrifuge General-purpose tabletop centrifuge General-purpose centrifuge IVD General-purpose centrifuge IVD General-purpose centrifuge IVD General-purpose centrifuge IVD General-purpose centrifuge IVD General-purpose centrifuge IVD General-purpose centrifuge IVD
Primary Device ID00810052861555
NIH Device Record Keye5c81ac0-a274-4c2e-a9d1-0cec7d18108e
Commercial Distribution StatusIn Commercial Distribution
Brand Name642VFD Plus Centrifuge, Selphyl US/CAN
Version Model Number00-027-055-001
Catalog Number00-027-055-001
Company DUNS022156957
Company NameDRUCKER DIAGNOSTICS
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 Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100810052861555 [Primary]

FDA Product Code

JQCCentrifuges (Micro, Ultra, Refrigerated) For Clinical Use

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-05-18
Device Publish Date2021-05-10

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