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Tissue-Tek® Lab Aid®

FDA UDI

Class I (US FDA UDI)

by Sakura Finetek USA, Inc

Identity

Trade Name
Tissue-Tek® Lab Aid® FDA UDI
Generic Name
Microscope slide cabinet FDA UDI
Device Name
Top Panel, Beige FDA UDI
Model / Reference
4013 FDA UDI
Description
Top Panel, Beige FDA UDI

Identifiers

Catalog Number
4013 FDA UDI
Primary DI / UDI-DI
08720177655620 FDA UDI
FDA Product Code
NNK FDA UDI
GMDN Term
Microscope slide cabinet FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3250 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: Microscope slide cabinet

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

Similar devices

Also classified as Microscope slide cabinet.

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 73445fe3-551d-4fd3-86f8-c4568108603b 35 fields · synced May 31, 2026