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Tissue-Tek Prisma®

FDA UDI

Class I (US FDA UDI)

by Sakura Finetek USA, Inc

Identity

Trade Name
Tissue-Tek Prisma® FDA UDI
Generic Name
Microscope slide coverslipper IVD FDA UDI
Device Name
Tissue-Tek Prisma® Link Between Tissue-Tek Prisma® and Tissue-Tek® Glas™ g2 FDA UDI
Model / Reference
6168 FDA UDI
Description
Tissue-Tek Prisma® Link Between Tissue-Tek Prisma® and Tissue-Tek® Glas™ g2 FDA UDI

Identifiers

Catalog Number
6168 FDA UDI
Primary DI / UDI-DI
00615233080585 FDA UDI
FDA Product Code
KIO FDA UDI
GMDN Term
Microscope slide coverslipper IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3800 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

Yes

FDA UDI

Category: Microscope slide coverslipper IVD

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

Similar devices

Also classified as Microscope slide coverslipper IVD.

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 3634c261-bce3-4102-9854-0454876416bb 35 fields · synced Jun 1, 2026