Tissue-Tek® Glas™ Coverslips, 24 x 60 mm (UDI 08720177654036)
Manufactured by Sakura Finetek Europe B.V.
Device Regulatory Overview
The Tissue-Tek® Glas™ Coverslips, 24 x 60 mm (Model/Catalog Number: 9582) is a medical device manufactured by Sakura Finetek Europe B.V.. This product is indexed under FDA Product Code / Category Classification W0503900202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9582
- Product Code / EMDN
- W0503900202
- Device Name
- Tissue-Tek® Glas™ Coverslips
- Database Sync Date
- 2026-08-09 16:30:28
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® Glas™ Coverslips, 24 x 60 mm?
The registered manufacturer of record for Tissue-Tek® Glas™ Coverslips, 24 x 60 mm is Sakura Finetek Europe B.V..
What is the Primary UDI-DI identifier for Tissue-Tek® Glas™ Coverslips, 24 x 60 mm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08720177654036.
What classification code is assigned to this device?
This device is registered under product classification code W0503900202.
Similar Classification Devices (W0503900202)
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