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Tissue-Tek® Quick-Ray™

FDA UDI

Class I (US FDA UDI)

by Sakura Finetek USA, Inc

Identity

Trade Name
Tissue-Tek® Quick-Ray™ FDA UDI
Generic Name
Tissue embedding mould IVD, reusable FDA UDI
Device Name
Recipient Base Mold; 3/case FDA UDI
Model / Reference
8020 FDA UDI
Description
Recipient Base Mold; 3/case FDA UDI

Identifiers

Catalog Number
8020 FDA UDI
Primary DI / UDI-DI
00615233081834 FDA UDI
FDA Product Code
KER FDA UDI
GMDN Term
Tissue embedding mould IVD, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3010 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tissue embedding mould IVD, reusable

Tissue-Tek® Quick-Ray™ by Sakura Finetek USA, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tissue embedding mould IVD, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sakura Finetek USA, Inc

Sources (1)

  • FDA UDI b9ef22d8-e177-48b7-a964-1aa43e773491 35 fields · synced Jun 8, 2026