Cyto-Tek® 2500 4300

GUDID 00615233078414

Cytocentrifuge

SAKURA FINETEK U.S.A., INC.

Cytological centrifuge
Primary Device ID00615233078414
NIH Device Record Key3cb8ce08-9965-41cd-a741-27a0b0f2f004
Commercial Distribution StatusIn Commercial Distribution
Brand NameCyto-Tek® 2500
Version Model Number4300
Catalog Number4300
Company DUNS179135769
Company NameSAKURA FINETEK U.S.A., INC.
Device Count1
DM Exempttrue
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(310)972-7800
Email[email protected]

Device Identifiers

Device Issuing AgencyDevice ID
GS100615233078414 [Primary]

FDA Product Code

IFBCYTOCENTRIFUGE

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-03-25
Device Publish Date2020-03-17

On-Brand Devices [Cyto-Tek® 2500]

006152330784211 mL Fluid Chamber Kit
00615233078414Cytocentrifuge

© 2020 FDA.report
This site is not affiliated with or endorsed by the FDA.