Tissue-Tek® TEC™ 6

FDA UDI

Class I (US FDA UDI)

by Sakura Finetek USA, Inc

Identity

Trade Name: Tissue-Tek® TEC™ 6 FDA UDI
Generic Name: Foot-switch, electrical FDA UDI
Device Name: Foot Pedal Switch FDA UDI
Model / Reference: 5785 FDA UDI
Description: Foot Pedal Switch FDA UDI

Identifiers

Catalog Number: 5785 FDA UDI
Primary DI / UDI-DI: 00615233079640 FDA UDI
FDA Product Code: IDW FDA UDI
GMDN Term: Foot-switch, electrical 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Foot-switch, electrical

Tissue-Tek® TEC™ 6 by Sakura Finetek USA, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Sakura Finetek USA, Inc

Sources (1)

FDA UDI 3a6e77ce-a003-4a90-a9ee-41dbeaa03eca 35 fields · synced May 30, 2026