eudamed_udi
Primary ID: 08806125613109
EASYPREP Slide chamber (UDI 08806125613109)
Manufactured by YD Diagnostics CORP.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EASYPREP Slide chamber - Primary ID 08806125613109
Device Regulatory Overview
The EASYPREP Slide chamber (Model/Catalog Number: EZ 07) is a medical device manufactured by YD Diagnostics CORP.. This product is indexed under FDA Product Code / Category Classification W0202059085 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EZ 07
- Product Code / EMDN
- W0202059085
- Device Name
- EASYPREP kits
- Database Sync Date
- 2026-08-09 16:46:10
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 EASYPREP Slide chamber?
The registered manufacturer of record for EASYPREP Slide chamber is YD Diagnostics CORP..
What is the Primary UDI-DI identifier for EASYPREP Slide chamber?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08806125613109.
What classification code is assigned to this device?
This device is registered under product classification code W0202059085.
Similar Classification Devices (W0202059085)
Other Devices by YD Diagnostics CORP.
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