Tissue-Tek® Quick-Ray™ 8020

GUDID 00615233081834

Recipient Base Mold; 3/case

SAKURA FINETEK U.S.A., INC.

Tissue embedding mould IVD, reusable
Primary Device ID00615233081834
NIH Device Record Keyb9ef22d8-e177-48b7-a964-1aa43e773491
Commercial Distribution StatusIn Commercial Distribution
Brand NameTissue-Tek® Quick-Ray™
Version Model Number8020
Catalog Number8020
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 Numberfalse
Manufacturing Datefalse
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
EmailTS@sakuraus.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100615233081834 [Primary]

FDA Product Code

KERCONTAINER, EMBEDDING

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 [Tissue-Tek® Quick-Ray™]

00615233081834Recipient Base Mold; 3/case
00615233081827Recipient Block, 5 mm
00615233081810Recipient Block, 3 mm
00615233081803Recipient Block, 2 mm
00615233081797Recipient Block, 1 mm
00615233081735Tissue Microarray System

Trademark Results [Tissue-Tek]

Mark Image

Registration | Serial
Company
Trademark
Application Date
TISSUE-TEK
TISSUE-TEK
72084436 0743380 Live/Registered
LAB-TEK PLASTICS CO.
1959-11-02

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