← Back to catalogue

Tissue-Tek® Paraform®

FDA UDI

Class I (US FDA UDI)

by Sakura Finetek USA, Inc

Identity

Trade Name
Tissue-Tek® Paraform® FDA UDI
Generic Name
Paraffin-based embedding medium IVD FDA UDI
Device Name
Processing/Embedding Medium Formula 3 FDA UDI
Model / Reference
7052 FDA UDI
Description
Processing/Embedding Medium Formula 3 FDA UDI

Identifiers

Catalog Number
7052 FDA UDI
Primary DI / UDI-DI
10615233081244 FDA UDI
FDA Product Code
IDZ FDA UDI
GMDN Term
Paraffin-based embedding medium IVD 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Paraffin-based embedding medium IVD

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

Similar devices

Also classified as Paraffin-based embedding medium IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Sakura Finetek USA, Inc

Sources (1)

  • FDA UDI 0d15f1ae-b74c-48e4-a51c-0b46db43ae57 35 fields · synced Jun 1, 2026