GUDIDData
eudamed_udi Primary ID: 08720177654159

Tissue-Tek® AutoWrite® Adhesive Ground Edges 90° Clipped Corner Slides, Green (UDI 08720177654159)

Manufactured by Sakura Finetek Europe B.V.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Tissue-Tek® AutoWrite® Adhesive Ground Edges 90° Clipped Corner Slides, Green - Primary ID 08720177654159

Device Regulatory Overview

The Tissue-Tek® AutoWrite® Adhesive Ground Edges 90° Clipped Corner Slides, Green (Model/Catalog Number: 9601) is a medical device manufactured by Sakura Finetek Europe B.V.. This product is indexed under FDA Product Code / Category Classification W0503900201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
9601
Product Code / EMDN
W0503900201
Device Name
Tissue-Tek® slides
Database Sync Date
2026-08-09 16:30:30

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Tissue-Tek® AutoWrite® Adhesive Ground Edges 90° Clipped Corner Slides, Green?

The registered manufacturer of record for Tissue-Tek® AutoWrite® Adhesive Ground Edges 90° Clipped Corner Slides, Green is Sakura Finetek Europe B.V..

What is the Primary UDI-DI identifier for Tissue-Tek® AutoWrite® Adhesive Ground Edges 90° Clipped Corner Slides, Green?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08720177654159.

What classification code is assigned to this device?

This device is registered under product classification code W0503900201.

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