Dermatophyte Test Agar (Derma TEST Agar) (UDI 05904708001107)
Manufactured by GRASO Zenon Sobiecki
Device Regulatory Overview
The Dermatophyte Test Agar (Derma TEST Agar) (Model/Catalog Number: 201452) is a medical device manufactured by GRASO Zenon Sobiecki. This product is indexed under FDA Product Code / Category Classification W0104030201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 201452
- Product Code / EMDN
- W0104030201
- Device Name
- Dermatophyte Test Agar (Derma TEST Agar)
- Database Sync Date
- 2026-08-09 17:53:30
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 Dermatophyte Test Agar (Derma TEST Agar)?
The registered manufacturer of record for Dermatophyte Test Agar (Derma TEST Agar) is GRASO Zenon Sobiecki.
What is the Primary UDI-DI identifier for Dermatophyte Test Agar (Derma TEST Agar)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05904708001107.
What classification code is assigned to this device?
This device is registered under product classification code W0104030201.
Similar Classification Devices (W0104030201)
Other Devices by GRASO Zenon Sobiecki
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