Microtome (UDI 06978114660028)
Manufactured by ZHEJIANG JINHUA KEDI INSTRUMENTAL EQUIPMENT CO.,LTD
Device Regulatory Overview
The Microtome (Model/Catalog Number: KD-202) is a medical device manufactured by ZHEJIANG JINHUA KEDI INSTRUMENTAL EQUIPMENT CO.,LTD. This product is indexed under FDA Product Code / Category Classification W02069099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KD-202
- Product Code / EMDN
- W02069099
- Device Name
- Microtome
- Database Sync Date
- 2026-08-09 16:29:06
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 Microtome?
The registered manufacturer of record for Microtome is ZHEJIANG JINHUA KEDI INSTRUMENTAL EQUIPMENT CO.,LTD.
What is the Primary UDI-DI identifier for Microtome?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06978114660028.
What classification code is assigned to this device?
This device is registered under product classification code W02069099.
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