Mannitol Salt Agar Plate (UDI 08606018771868)
Manufactured by DRUŠTVO ZA TRGOVINU I USLUGE PROMEDIA DOO KIKINDA
Device Regulatory Overview
The Mannitol Salt Agar Plate (Model/Catalog Number: PRM118V240) 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
- PRM118V240
- Product Code / EMDN
- W0104010405
- Device Name
- Mannitol Salt Agar Plate
- Database Sync Date
- 2026-08-09 17:53:47
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 Mannitol Salt Agar Plate?
The registered manufacturer of record for Mannitol Salt Agar Plate is DRUŠTVO ZA TRGOVINU I USLUGE PROMEDIA DOO KIKINDA.
What is the Primary UDI-DI identifier for Mannitol Salt Agar Plate?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08606018771868.
What classification code is assigned to this device?
This device is registered under product classification code W0104010405.
Similar Classification Devices (W0104010405)
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