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 ID: 00615233081834
• NIH Device Record Key: b9ef22d8-e177-48b7-a964-1aa43e773491
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tissue-Tek® Quick-Ray™
• Version Model Number: 8020
• Catalog Number: 8020
• Company DUNS: 179135769
• Company Name: SAKURA FINETEK U.S.A., INC.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(310)972-7800
• Email: TS@sakuraus.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00615233081834 [Primary]

FDA Product Code

• KER: CONTAINER, EMBEDDING

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-03-25
• Device Publish Date: 2020-03-17

On-Brand Devices [Tissue-Tek® Quick-Ray™]

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