eudamed_udi
Primary ID: 05904708004955
Dermatophytes Agar Modified (UDI 05904708004955)
Manufactured by GRASO Zenon Sobiecki
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Dermatophytes Agar Modified - Primary ID 05904708004955
Device Regulatory Overview
The Dermatophytes Agar Modified (Model/Catalog Number: TN2102) 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
- TN2102
- Product Code / EMDN
- W0104030201
- Device Name
- Dermatophytes Agar Modified
- Database Sync Date
- 2026-08-09 18:08:49
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 Dermatophytes Agar Modified?
The registered manufacturer of record for Dermatophytes Agar Modified is GRASO Zenon Sobiecki.
What is the Primary UDI-DI identifier for Dermatophytes Agar Modified?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05904708004955.
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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