gudid
Primary ID: 4017
Tissue-Tek Lab Aid (UDI 4017)
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 Lab Aid - Primary ID 4017
Device Regulatory Overview
The Tissue-Tek Lab Aid (Model/Catalog Number: 4017) is a medical device manufactured by SAKURA FINETEK U.S.A., INC.. This product is indexed under FDA Product Code / Category Classification NNK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4017
- Product Code / EMDN
- NNK
- Device Name
- Drawer Section 7x76x50 mm, Beige
- Database Sync Date
- 2026-08-09 09:26:43
Full Regulatory Attributes
🔒 Token Gated
{
"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 Lab Aid?
The registered manufacturer of record for Tissue-Tek Lab Aid is SAKURA FINETEK U.S.A., INC..
What is the Primary UDI-DI identifier for Tissue-Tek Lab Aid?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 4017.
What classification code is assigned to this device?
This device is registered under product classification code NNK.
Similar Classification Devices (NNK)
Other Devices by SAKURA FINETEK U.S.A., INC.
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