Tissue-Tek VIP® 5990

GUDID 10615233080155

Fixative

SAKURA FINETEK U.S.A., INC.

10% Formaldehyde solution IVD

• Primary Device ID: 10615233080155
• NIH Device Record Key: 9b001f9f-b544-4579-a0c7-8bef153bce79
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tissue-Tek VIP®
• Version Model Number: 5990
• Catalog Number: 5990
• Company DUNS: 179135769
• Company Name: SAKURA FINETEK U.S.A., INC.
• Device Count: 4
• 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: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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	00615233080158 [Unit of Use]
GS1	10615233080155 [Primary]

FDA Product Code

• IFP: FORMALIN, NEUTRAL BUFFERED

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: 2019-12-23
• Device Publish Date: 2019-12-15

On-Brand Devices [Tissue-Tek VIP®]

• 10615233080155: Fixative
• 00615233080165: Fixative, 5 Gallon Cube
• 00615233080141: Fixative, 2.5 Gallon Cube
• 00615233080172: Spigot