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Tissue-Tek® Glas™ g2

FDA UDI

Class I (US FDA UDI)

by Sakura Finetek USA, Inc

Identity

Trade Name
Tissue-Tek® Glas™ g2 FDA UDI
Generic Name
Microscope slide holder, preparation/staining FDA UDI
Device Name
Coverslips 24 x 60 mm; 200 coverslips; 5 holders/case FDA UDI
Model / Reference
6417 FDA UDI
Description
Coverslips 24 x 60 mm; 200 coverslips; 5 holders/case FDA UDI

Identifiers

Catalog Number
6417 FDA UDI
Primary DI / UDI-DI
00615233080646 FDA UDI
FDA Product Code
KES FDA UDI
GMDN Term
Microscope slide holder, preparation/staining 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Microscope slide coverslip IVDMicroscope slide holder, preparation/staining

Tissue-Tek® Glas™ g2 by Sakura Finetek USA, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Microscope slide holder, preparation/staining.

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 699ecafd-2670-4167-8601-827bf9dcafe0 35 fields · synced Jun 1, 2026