eudamed_udi
Primary ID: 08059616660438
APE ELITE (UDI 08059616660438)
Manufactured by DAS Srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for APE ELITE - Primary ID 08059616660438
Device Regulatory Overview
The APE ELITE (Model/Catalog Number: OR-105401) is a medical device manufactured by DAS Srl. This product is indexed under FDA Product Code / Category Classification W0201020102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- OR-105401
- Product Code / EMDN
- W0201020102
- Device Name
- AP ELISA
- Database Sync Date
- 2026-08-09 16:59:09
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 APE ELITE?
The registered manufacturer of record for APE ELITE is DAS Srl.
What is the Primary UDI-DI identifier for APE ELITE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08059616660438.
What classification code is assigned to this device?
This device is registered under product classification code W0201020102.
Similar Classification Devices (W0201020102)
Other Devices by DAS Srl
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