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Tissue-Tek®

FDA UDI

Class I (US FDA UDI)

by Sakura Finetek USA, Inc

Identity

Trade Name
Tissue-Tek® FDA UDI
Generic Name
Barcode reader FDA UDI
Device Name
Barcode Reader System for Coverslippers FDA UDI
Model / Reference
6508 FDA UDI
Description
Barcode Reader System for Coverslippers FDA UDI

Identifiers

Catalog Number
6508 FDA UDI
Primary DI / UDI-DI
00615233080837 FDA UDI
FDA Product Code
KIM FDA UDI
GMDN Term
Barcode reader FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3400 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Barcode reader

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

Similar devices

Also classified as Barcode reader.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 27cd428c-5399-4f28-92f1-0ee10b2ede86 35 fields · synced May 30, 2026