Endo Agar Plate (UDI 08606018770427)
Manufactured by DRUŠTVO ZA TRGOVINU I USLUGE PROMEDIA DOO KIKINDA
Device Regulatory Overview
The Endo Agar Plate (Model/Catalog Number: PRM029V240) is a medical device manufactured by DRUŠTVO ZA TRGOVINU I USLUGE PROMEDIA DOO KIKINDA. This product is indexed under FDA Product Code / Category Classification W0104010405 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PRM029V240
- Product Code / EMDN
- W0104010405
- Device Name
- Endo Agar Plate
- Database Sync Date
- 2026-08-09 16:48:33
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 Endo Agar Plate?
The registered manufacturer of record for Endo Agar Plate is DRUŠTVO ZA TRGOVINU I USLUGE PROMEDIA DOO KIKINDA.
What is the Primary UDI-DI identifier for Endo Agar Plate?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08606018770427.
What classification code is assigned to this device?
This device is registered under product classification code W0104010405.
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