eudamed_udi
Primary ID: 04260678680003
KleeYa® Instrument (UDI 04260678680003)
Manufactured by STRATEC SE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KleeYa® Instrument - Primary ID 04260678680003
Device Regulatory Overview
The KleeYa® Instrument (Model/Catalog Number: 10108093) is a medical device manufactured by STRATEC SE. This product is indexed under FDA Product Code / Category Classification W0201020102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10108093
- Product Code / EMDN
- W0201020102
- Device Name
- KleeYa® Instrument
- Database Sync Date
- 2026-08-09 16:28:51
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of KleeYa® Instrument?
The registered manufacturer of record for KleeYa® Instrument is STRATEC SE.
What is the Primary UDI-DI identifier for KleeYa® Instrument?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260678680003.
What classification code is assigned to this device?
This device is registered under product classification code W0201020102.
Similar Classification Devices (W0201020102)
Other Devices by STRATEC SE
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint