gudid
Primary ID: 4782
Tissue-Tek Accu-Edge (UDI 4782)
Manufactured by SAKURA FINETEK U.S.A., INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Tissue-Tek Accu-Edge - Primary ID 4782
Device Regulatory Overview
The Tissue-Tek Accu-Edge (Model/Catalog Number: 4782) is a medical device manufactured by SAKURA FINETEK U.S.A., INC.. This product is indexed under FDA Product Code / Category Classification JOK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4782
- Product Code / EMDN
- JOK
- Device Name
- Autopsy Blade, 100 mm; 5/case
- Database Sync Date
- 2026-08-09 09:29:18
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Tissue-Tek Accu-Edge?
The registered manufacturer of record for Tissue-Tek Accu-Edge is SAKURA FINETEK U.S.A., INC..
What is the Primary UDI-DI identifier for Tissue-Tek Accu-Edge?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 4782.
What classification code is assigned to this device?
This device is registered under product classification code JOK.
Similar Classification Devices (JOK)
Other Devices by SAKURA FINETEK U.S.A., INC.
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