Panel 1 (UDI 04251342600014)
Manufactured by MEDIWISS ANALYTIC GmbH Gesellschaft für angewandte in-vitro Analytik
Device Regulatory Overview
The Panel 1 (Model/Catalog Number: 0001) is a medical device manufactured by MEDIWISS ANALYTIC GmbH Gesellschaft für angewandte in-vitro Analytik. This product is indexed under FDA Product Code / Category Classification W01020205 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0001
- Product Code / EMDN
- W01020205
- Device Name
- AllergyScreen®/AlleisaScreen®
- Database Sync Date
- 2026-08-09 16:28:48
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 Panel 1?
The registered manufacturer of record for Panel 1 is MEDIWISS ANALYTIC GmbH Gesellschaft für angewandte in-vitro Analytik.
What is the Primary UDI-DI identifier for Panel 1?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251342600014.
What classification code is assigned to this device?
This device is registered under product classification code W01020205.
Similar Classification Devices (W01020205)
Other Devices by MEDIWISS ANALYTIC GmbH Gesellschaft für angewandte in-vitro Analytik
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